"68382-535-30" National Drug Code (NDC)

Minocycline Hydrochloride 10 BLISTER PACK in 1 CARTON (68382-535-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
(Zydus Pharmaceuticals (USA) Inc.)

NDC Code68382-535-30
Package Description10 BLISTER PACK in 1 CARTON (68382-535-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC68382-535
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
Strength135
Strength Unitmg/1
Pharmacy ClassesDecreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS]

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