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"0187-1101-09" National Drug Code (NDC)

Tretinoin 20 g in 1 TUBE (0187-1101-09)
(Valeant Pharmaceuticals North America LLC)

NDC Code0187-1101-09
Package Description20 g in 1 TUBE (0187-1101-09)
Product NDC0187-1101
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTretinoin
Non-Proprietary NameTretinoin
Dosage FormGEL
UsageTOPICAL
Start Marketing Date20090801
End Marketing Date20160531
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA022070
ManufacturerValeant Pharmaceuticals North America LLC
Substance NameTRETINOIN
Strength.05
Strength Unitg/100g
Pharmacy ClassesRetinoid [EPC],Retinoids [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0187-1101-09





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