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"70756-052-12" National Drug Code (NDC)

Famotidine 1000 TABLET in 1 BOTTLE (70756-052-12)
(Lifestar Pharma LLC)

NDC Code70756-052-12
Package Description1000 TABLET in 1 BOTTLE (70756-052-12)
Product NDC70756-052
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20231019
Marketing Category NameANDA
Application NumberANDA075302
ManufacturerLifestar Pharma LLC
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70756-052-12





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