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"68788-9834-2" National Drug Code (NDC)

Tretinoin 20 g in 1 TUBE (68788-9834-2)
(Preferred Pharmaceuticals, Inc)

NDC Code68788-9834-2
Package Description20 g in 1 TUBE (68788-9834-2)
Product NDC68788-9834
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTretinoin
Non-Proprietary NameTretinoin
Dosage FormCREAM
UsageTOPICAL
Start Marketing Date20120329
Marketing Category NameANDA
Application NumberANDA075265
ManufacturerPreferred Pharmaceuticals, Inc
Substance NameTRETINOIN
Strength.5
Strength Unitmg/g
Pharmacy ClassesRetinoid [EPC],Retinoids [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68788-9834-2





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