Label: DOXYCYCLINE tablet, film coated
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Contains inactivated NDC Code(s)
NDC Code(s): 51376-780-10 - Packager: Blessings International
- Category: HUMAN PRESCRIPTION DRUG LABEL
Drug Label Information
Updated January 22, 2020
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- PRINCIPAL DISPLAY PANEL - 100 mg Tablet Bottle Label
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INGREDIENTS AND APPEARANCE
DOXYCYCLINE
doxycycline tablet, film coatedProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:51376-780 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Doxycycline (UNII: N12000U13O) (DOXYCYCLINE ANHYDROUS - UNII:334895S862) DOXYCYCLINE ANHYDROUS 100 mg Inactive Ingredients Ingredient Name Strength Magnesium Stearate (UNII: 70097M6I30) Isopropyl Alcohol (UNII: ND2M416302) Methylene Chloride (UNII: 588X2YUY0A) Microcrystalline Cellulose (UNII: OP1R32D61U) Talc (UNII: 7SEV7J4R1U) Starch, Potato (UNII: 8I089SAH3T) Product Characteristics Color ORANGE Score no score Shape ROUND Size 10mm Flavor Imprint Code DOXYC Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51376-780-10 1000 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/01/2008 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Export only 05/01/2008 Labeler - Blessings International (064965742) Establishment Name Address ID/FEI Business Operations Blessings International 064965742 MANUFACTURE(51376-780)
