"68382-531-01" National Drug Code (NDC)

Minocycline Hydrochloride 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-531-01)
(Zydus Pharmaceuticals (USA) Inc.)

NDC Code68382-531-01
Package Description100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-531-01)
Product NDC68382-531
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMinocycline Hydrochloride
Non-Proprietary NameMinocycline Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20180307
Marketing Category NameANDA
Application NumberANDA203553
ManufacturerZydus Pharmaceuticals (USA) Inc.
Substance NameMINOCYCLINE HYDROCHLORIDE
Strength45
Strength Unitmg/1
Pharmacy ClassesDecreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS]

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