NDC 63629-2229

Minocycline

Minocycline

Minocycline is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Minocycline Hydrochloride.

Product ID63629-2229_3dcbda95-a1c9-48ed-bec2-d5e07caef115
NDC63629-2229
Product TypeHuman Prescription Drug
Proprietary NameMinocycline
Generic NameMinocycline
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2003-04-16
Marketing CategoryANDA /
Application NumberANDA065131
Labeler NameBryant Ranch Prepack
Substance NameMINOCYCLINE HYDROCHLORIDE
Active Ingredient Strength50 mg/1
Pharm ClassesTetracycline-class Drug [EPC], Tetracyclines [CS]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 63629-2229-1

100 TABLET in 1 BOTTLE (63629-2229-1)
Marketing Start Date2021-03-22
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Minocycline" or generic name "Minocycline"

NDCBrand NameGeneric Name
42291-589MinocyclineMinocycline
42291-591MinocyclineMinocycline
49884-511MinocyclineMinocycline
49884-512MinocyclineMinocycline
49884-513MinocyclineMinocycline
57664-854MinocyclineMinocycline Hydrochloride
57664-855MinocyclineMinocycline Hydrochloride
57664-856MinocyclineMinocycline Hydrochloride
63629-2228MinocyclineMinocycline
63629-2229MinocyclineMinocycline
69489-201AMZEEQMinocycline
72356-101AMZEEQMinocycline
69489-212ZILXIMinocycline
72356-103ZILXIMinocycline

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