"61919-808-30" National Drug Code (NDC)

Propranolol Hydrochloride 30 TABLET in 1 BOTTLE (61919-808-30)
(DIRECT RX)

NDC Code61919-808-30
Package Description30 TABLET in 1 BOTTLE (61919-808-30)
Product NDC61919-808
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePropranolol Hydrochloride
Non-Proprietary NamePropranolol Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20140101
Marketing Category NameANDA
Application NumberANDA078955
ManufacturerDIRECT RX
Substance NamePROPRANOLOL HYDROCHLORIDE
Strength40
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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