Label: MORPHINUM- morphine pellet
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Contains inactivated NDC Code(s)
NDC Code(s): 10191-1003-2 - Packager: REMEDY MAKERS
- Category: HUMAN PRESCRIPTION DRUG LABEL
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated August 18, 2015
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- SPL UNCLASSIFIED SECTION
- WARNING
- INDICATION:
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WARNING
Use only if cap and seal are unbroken. Keep this and all medication out of reach of children. If symptoms persist for more than 3 days or worsen, discontinue (STOP) use and consult your physician. As with any drug. If you are pregnant or nursing (breast-feeding) a baby, seek the advise of a health professional before using this product. Store tightly closed in a cool area.
- Directions (adult/children)
- Inactive Ingredients
- Other Information
- Questions or comments
- WARNINGS AND PRECAUTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MORPHINUM
morphine pelletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:10191-1003 Route of Administration SUBLINGUAL DEA Schedule CII Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ABT-925 ANHYDROUS FREE BASE (UNII: E6CKI5C54O) (ABT-925 ANHYDROUS FREE BASE - UNII:E6CKI5C54O) ABT-925 ANHYDROUS FREE BASE 9 [hp_X] Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) SUCROSE (UNII: C151H8M554) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10191-1003-2 154 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/30/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/30/2015 Labeler - REMEDY MAKERS (018543582)