"0115-2122-14" National Drug Code (NDC)

Demeclocycline Hydrochloride 48 TABLET, FILM COATED in 1 BOTTLE (0115-2122-14)
(Global Pharmaceuticals, Division of Impax Laboratories, Inc.)

NDC Code0115-2122-14
Package Description48 TABLET, FILM COATED in 1 BOTTLE (0115-2122-14)
Product NDC0115-2122
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDemeclocycline Hydrochloride
Non-Proprietary NameDemeclocycline Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20040322
Marketing Category NameANDA
Application NumberANDA065094
ManufacturerGlobal Pharmaceuticals, Division of Impax Laboratories, Inc.
Substance NameDEMECLOCYCLINE HYDROCHLORIDE
Strength300
Strength Unitmg/1
Pharmacy ClassesTetracycline-class Antimicrobial [EPC],Tetracyclines [Chemical/Ingredient]

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