Label: BIOPAR DELTA-FORTE- 1 nf units, 50 mcg cbl, 2.5 mg f-thf, 1 mg pteglu-, 7 mg me-thf capsule

  • NDC Code(s): 64661-793-30
  • Packager: Jaymac Pharmacueticals LLC
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated October 19, 2020

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  • DESCRIPTION

       [1 NF Units] [50 mcg CBl] [2.5 mg F-THf] [1 mg PteGlu-] [7 mg Me-THf]

       Prescription Hematopoietic Preparation For Therapeutic Use

       Multiphasic Softgels (30ct carton)

       NDC 64661-793-30
       Rx ONLY

       BioparTMdelta-FORTE is an orally administered prescription hematopoietic preparation for therapeutic use formulated for adult macrocytic anemia patients – specifically including pernicious anemia patients, ages 12 and up, who are under specific direction and monitoring of cobalamin and folate status by a physician. A recent study+ suggested that BioparTM delta-FORTE was effective in lowering homocysteine levels in patients that are positive for MTHFR (methylenetetrahydrofolate reductase polymorphism). BioparTM delta-FORTE may be taken by women of childbearing age. BioparTM delta-FORTE may be taken by geriatric patients where compliance is an issue.

        + ClinicalTrials.gov identifier: NCT02709668, Correlation of Clinical Response With Homocysteine Reduction During Therapy With Reduced B Vitamins in Patients with MDD Who Are Positive for MTHFR C677T or A1298C Polymorphism.

  • INGREDIENTS

       Cobalamin-intrinsic factor concentrate (non-inhibitory)1 .............................................................................................. 1 NF Units§

       Adenosylcobalamin (coenzyme B12) .............................................................................................................................. 50 mcg

       Formyl folic acid, L-FTHf .............................................................................................................................................. 2.5 mg2

       Reduced folic acid, DHf- ................................................................................................................................................. 1 mg2

       Methyl folic acid, L-MeTHf ............................................................................................................................................... 7 mg2

          1 50 mcg Vitamin B12 (activity equivalent) and 50 mg of intrinsic factor concentrate§ from ultra-purified, porcine-derived stomach substance from a porcine, disease-free country; together these equal 1 NF Units. Cobalamin has hematopoietic activity apparently identical to that of the anti-anemia factor in purified liver-stomach extract

          2 15 mg DFE DeltaFolate™ (total folates) of which 9 mg DFE is from l-methylfolate magnesium (molar equivalent) from amorphous, diastereoisomerically pure l-methylfolate (less than 1% d-isomer)

  • INACTIVES

    FUNCTIONAL EXCIPIENTS:

          25 mg ascorbates4a (24 mg magnesium l-ascorbate, 1 mg zinc l-ascorbate) [antioxidant], 13.6 mg chelates (FeGC3 as ferrous glycine cysteinate subsisting of 1.5 mg elemental iron4a) [colorant].


    OTHER EXCIPIENTS:

          Annatto [colorant], betaine (trimethylglycine) [acidifier], citrates (citric acid, sodium citrate) [stabilizers], flavin adenine dinucleotide (B2-vitamer)4b, gelatin (bovine), glycerine, nicotinamide adenine dinucleotide hydride (B3-vitamer)4b, phospholipids (sunflower lecithin, phosphatidylserine-docosahexaenoic acid complex5) [emulsifiers], piperine [bioavailability enhancer], purified water, pyridoxal 5’ phosphate (B6-vitamer)4bthiamine pyrophosphate (B1-vitamer)4b, ubidecarenone [antioxidant], yellow beeswax.

          3 Pure amino acid, cysteinated iron chelate as AminoFerTM under exclusive license by Viva Pharmaceuticals, Canada, U.S. Patent #7341708

          4a 30% daily value (DV) of VITAMIN C, and 10% DV IRON for geriatric patients.

          4b Contains less than 2% (<25 mcg/each) of vitamins B1, B2, B3 and B6.

          5 Contains at least 12 mg phosphatidylserine (PS) – of which approximately 6.4 mg as PS-DHA, and less than 1% EPA (<800 mcg PS-EPA)

  • CONTAINS

       FISH/KRILL/PORCINE (Intrinsic Factor/Cobalamin)/SOY

       Certified 3rd-party GLUTEN-FREE. No artificial colorants. No dairy, wheat, sugar or egg

  • INDICATIONS & USAGE

       BioparTMdelta-FORTE is indicated in the treatment of pernicious anemia and the prevention of folate deficiency;

       BioparTM delta-FORTE is specifically indicated as a primary and adjunctive treatment in pernicious anemia patients having idiosyncrasy or sensitivity to parenteral administration - or when parental therapy is refused;

       BioparTM delta-FORTE is further indicated in the maintenance of normal hematologic status (hematopoiesis) in macrocytic anemia conditions which are caused by either cobalamin and/or folate deficiency, and where increased intrinsic factor is desired - including:

          1. Malabsorption of cobalamin resulting from structural or functional damage to the stomach - where intrinsic factor is secreted, or to the ileum, where intrinsic factor facilitates cobalamin absorption. Folate deficiency in these patients is usually more severe than cobalamin deficiency;

          2. Genetic polymorphisms such as MTHFR that impede folate metabolism and the effective use of synthetic folic acid (oxidized form); and

          3. Inadequate secretion of intrinsic factor, resulting from lesions that destroy the gastric mucosa (ingestion of corrosives, extensive neoplasia), and a number of conditions associated with a variable degree of gastric atrophy (certain endocrine disorders, iron deficiency, and subtotal gastrectomy). Total gastrectomy always produces cobalamin deficiency. Structural lesions leading to cobalamin deficiency include regional ileitis, ileal resections, malignancies, etc

  • MECHANISM OF ACTION

    COBALAMIN [treatment]; FOLATE [prevention]; INTRINSIC FACTOR [facilitator] -

    Cobalamin is essential for the synthesis of methionine from homocysteine - a reaction which also requires folate. In the absence of cobalamin - ie, cobalamin deficiency, tetrahydrofolate cannot be regenerated from l-methylfolic acid, and a functional folate deficiency occurs - ie, “methyl trap hypothesis”. Gastrointestinal absorption of cobalamin depends on the presence of sufficient intrinsic factor, and lack of intrinisic factor results in cobalamin deficiency.

  • DOSAGE & ADMINISTRATION

       The adult dose is one capsule daily preferably on an empty stomach.

       A deficiency of cobalamin may present first as folate deficiency - which is why folate supplementation may mask the symptoms that would normally result and also why advanced folate supplementation requires licensed medical supervision; because of this, reticulocyte plasma count, cobalamin and folate must be obtained prior to treatmentRequirements of cobalamin and/or folate in excess of normal (due to pregnancy, thyrotoxicosis, hemolytic anemia, hemorrhage, malignancy, hepatic and renal disease) can usually be met with oral supplementation. 

       As a general rule - in Pernicious Anemia patients, treatment will be required for the remainder of the patient’s life, and usually requires weekly or monthly injections at the doctor's office. Patients that are non-compliant with parenteral therapy (injections) may use this product as a substitute ONLY UNDER THE DIRECT SUPERVISION OF A LICENSED MEDICAL PRACTITIONER. 

  • ADVERSE REACTIONS

       Mild transient diarrhea, polycythemia vera, itching, transitory exanthema, feeling of swelling of entire body may occur with administration of cobalamin. Allergic sensitization has been reported following both oral and parenteral administration of folate.

       Sensitivity to porcine intrinsic factor derived from liver substance has been reported in patients, and may occur at any time; BioparTMdelta-FORTE contains a non-inhibitory form of intrinsic factor that is not derived from liver substance but rather just the mucosa (stomach substance) - in which such senstitivity is less likely to occur, however caution is advised and continuous monitoring under licensed medical supervision is required.

  • BOXED WARNING (What is this?)

    WARNING

    USE OF THIS PRODUCT WITHOUT DIRECT SUPERVISION OF A PHYSICIAN IS DANGEROUS;
    Some patients afflicted with pernicious anemia may or not respond to the orally ingested vitamin B12, and there is no known way to predict which patients may respond and which patients may cease to respond;
    Periodic examinations and laboratory studies of pernicious anemia patients are essential and recommended; and -
    The parenteral administration of (cyano)cobalamin - or vitamin B12, is generally recognized as a fully effective treatment of pernicious anemia. Parenteral alkyl-cobalamin preparations have not been and are not authorized for use except by or on the prescription of a physician.

  • PRECAUTIONS

    GENERAL:

          0.1 mg or more of folic acid daily may obscure pernicious anemia in that the hematological remission may occur while neurological manifestations remain progressive. The safe tolerable limit for folic acid (in preparations) is 1 mg [emphasis added];

          Folic acid is not a substitute for vitamin B12 - although it may improve vitamin B12-deficient anemias. Exclusive use of folic acid in treating vitamin B12-deficient anemias could result in progressive and irreversible neurologic damage. Specifically, vitamin B12 deficiency allowed to progress over 3 months may produce permanent degenerative lesions of the spinal cord - as observed when folate therapy is used as the only hematopoietic agent;

          Doses of vitamin B12 exceeding 10 mcg daily may produce hematologic response in patients with folate deficiency. Indiscriminate administration may mask the true diagnosis; and -

          A dietary deficiency of only vitamin B12 is rare; multiple vitamin deficiency is expected in any dietary deficiency. No single regimen fits all cases, and the status of the patient observed in follow-up is the final criterion for adequacy of therapy.

    DRUG INTERACTIONS:

          Colchicine, para-aminosalicylic acid, and heavy alcohol intake for longer than 2 weeks may produce malabsorption of cobalamin.

          Epileptic, antineoplastic and Parkinson's medications are cautioned in the concimant use with folate supplementation.

  • HOW SUPPLIED

       BioparTM delta-FORTE is supplied as oval, annatto (”orangish-brown”) multiphasic softgels* with imprint "7N3". Provided as a carton with 30 softgels in blister cards. NDC 64661-793-30.

  • REGULATORY

    BioparTMdelta-FORTE is regulated as a drug to ensure it's use is under medical supervision, and because of this, advanced folate supplementation is possible [21 CFR 250.201].

  • STORAGE AND HANDLING

       Call your medical practitioner about side effects. You may report side effects by calling (337) 662-5962.

       KEEP THIS OUT OF THE REACH OF CHILDREN.

       (Tamper Evident: Do not use if seal is broken or missing)

    Do not exceed the recommended dose.

       STORAGE: Store at 20 ̊-25 ̊ C (68 ̊-77 ̊ F)

       CAUTION: FEDERAL LAW PROHIBITS DISPENSING WITHOUT A PRESCRIPTION

       [Rx ONLY]

    PATENTS: Patent(s) pending.

    TRADEMARKS: BioparTMdelta-FORTE is a registered mark of JayMac Pharmaceuticals. DeltaFolateTM is a use-trademark of Jaymac Pharmaceuticals.

       JAYMAC Pharmaceuticals, LLC

       Sunset, LA 70584

       MANUFACTURED AND/OR PACKAGED IN USA/CANADA

       Revision

       August 26, 2020

  • CARTON IMAGES

    carton 1

    carton 2

    carton 3

    carton 4

    carton 5

  • PACKAGE INSERT

    Package Insert

  • PILL/CAPSULE IMAGE

    Pill image

  • BLISTER CARD

    Blister card

  • INGREDIENTS AND APPEARANCE
    BIOPAR DELTA-FORTE 
    1 nf units, 50 mcg cbl, 2.5 mg f-thf, 1 mg pteglu-, 7 mg me-thf capsule
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:64661-793
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    INTRINSIC FACTOR (UNII: 70BT6OQT2Q) (INTRINSIC FACTOR - UNII:70BT6OQT2Q) INTRINSIC FACTOR50 mg
    COBALAMIN (UNII: 8406EY2OQA) (COBALAMIN - UNII:8406EY2OQA) COBALAMIN50 ug
    COBAMAMIDE (UNII: F0R1QK73KB) (COBAMAMIDE - UNII:F0R1QK73KB) COBAMAMIDE50 ug
    levoLEUCOVORIN (UNII: 990S25980Y) (LEVOLEUCOVORIN - UNII:990S25980Y) levoLEUCOVORIN2.5 mg
    DIHYDROFOLIC ACID (UNII: KXP0KNM559) (FOLIC ACID - UNII:935E97BOY8) FOLIC ACID1 mg
    LEVOMEFOLATE MAGNESIUM (UNII: 1VZZ62R081) (LEVOMEFOLIC ACID - UNII:8S95DH25XC) LEVOMEFOLIC ACID7 mg
    Inactive Ingredients
    Ingredient NameStrength
    FERROUS CYSTEINE GLYCINATE (UNII: 8B4OP7RK5N) 13.6 mg
    1,2-DOCOSAHEXANOYL-SN-GLYCERO-3-PHOSPHOSERINE CALCIUM (UNII: 6WJM73T46K) 6.4 mg
    1,2-ICOSAPENTOYL-SN-GLYCERO-3-PHOSPHOSERINE CALCIUM (UNII: 9ABD9DRK7B) 800 ug
    PHOSPHATIDYL SERINE (UNII: 394XK0IH40) 12 mg
    PYRIDOXAL PHOSPHATE ANHYDROUS (UNII: F06SGE49M6) 25 ug
    FLAVIN ADENINE DINUCLEOTIDE (UNII: ZC44YTI8KK) 25 ug
    NADH (UNII: 4J24DQ0916) 25 ug
    COCARBOXYLASE (UNII: Q57971654Y) 25 ug
    MAGNESIUM ASCORBATE (UNII: 0N1G678593) 24 mg
    ZINC ASCORBATE (UNII: 9TI35313XW) 1 mg
    RIBOFLAVIN (UNII: TLM2976OFR) 5 mg
    MAGNESIUM L-THREONATE (UNII: 1Y26ZZ0OTM) 1 mg
    BETAINE (UNII: 3SCV180C9W) 500 ug
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) 1.83 mg
    SODIUM CITRATE (UNII: 1Q73Q2JULR) 3.67 mg
    ANNATTO (UNII: 6PQP1V1B6O)  
    GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)  
    OLIVE OIL (UNII: 6UYK2W1W1E)  
    PIPERINE (UNII: U71XL721QK)  
    WATER (UNII: 059QF0KO0R)  
    UBIDECARENONE (UNII: EJ27X76M46)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    Product Characteristics
    Colorbrown (ORANGISH-BROWN) Scoreno score
    ShapeOVALSize16mm
    FlavorImprint Code 7N3
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64661-793-3030 in 1 CARTON09/01/2020
    11 in 1 BLISTER PACK; Number of Units = 3; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/01/2020
    Labeler - Jaymac Pharmacueticals LLC (830767260)
    Registrant - Jaymac Pharmacueticals LLC (830767260)
    Establishment
    NameAddressID/FEIBusiness Operations
    Viva Pharmaceuticals INC253288898manufacture(64661-793)