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"51672-1395-0" National Drug Code (NDC)

Tretinoin 1 TUBE in 1 CARTON (51672-1395-0) > 20 g in 1 TUBE
(Taro Pharmaceuticals U.S.A., Inc.)

NDC Code51672-1395-0
Package Description1 TUBE in 1 CARTON (51672-1395-0) > 20 g in 1 TUBE
Product NDC51672-1395
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTretinoin
Non-Proprietary NameTretinoin
Dosage FormCREAM
UsageTOPICAL
Start Marketing Date20190122
Marketing Category NameANDA
Application NumberANDA211645
ManufacturerTaro Pharmaceuticals U.S.A., Inc.
Substance NameTRETINOIN
Strength1
Strength Unitmg/g
Pharmacy ClassesRetinoid [EPC], Retinoids [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51672-1395-0





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