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"68788-7039-2" National Drug Code (NDC)

Tretinoin 1 TUBE in 1 CARTON (68788-7039-2) > 20 g in 1 TUBE
(Preferred Pharmaceuticals Inc.)

NDC Code68788-7039-2
Package Description1 TUBE in 1 CARTON (68788-7039-2) > 20 g in 1 TUBE
Product NDC68788-7039
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTretinoin
Non-Proprietary NameTretinoin
Dosage FormCREAM
UsageTOPICAL
Start Marketing Date20171027
Marketing Category NameANDA
Application NumberANDA075265
ManufacturerPreferred Pharmaceuticals Inc.
Substance NameTRETINOIN
Strength.5
Strength Unitmg/g
Pharmacy ClassesRetinoid [EPC],Retinoids [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68788-7039-2





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