Label: ANATRA- anas barbariae tablet
- NDC Code(s): 83641-001-01, 83641-001-02
- Packager: Anatra LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated September 15, 2023
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INGREDIENTS AND APPEARANCE
ANATRA
anas barbariae tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83641-001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY) (CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE - UNII:RN2HC612GY) CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE 200 [hp_C] Inactive Ingredients Ingredient Name Strength BETA CAROTENE (UNII: 01YAE03M7J) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561) DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) MAGNESIUM STEARATE (UNII: 70097M6I30) REBAUDIOSIDE A (UNII: B3FUD0528F) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color orange Score no score Shape ROUND Size 12mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83641-001-01 30 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/01/2023 2 NDC:83641-001-02 60 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/01/2023 Labeler - Anatra LLC (121482372)