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"53002-8101-1" National Drug Code (NDC)

Tretinoin 20 g in 1 TUBE (53002-8101-1)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-8101-1
Package Description20 g in 1 TUBE (53002-8101-1)
Product NDC53002-8101
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTretinoin
Non-Proprietary NameTretinoin
Dosage FormCREAM
UsageTOPICAL
Start Marketing Date20170615
Marketing Category NameANDA
Application NumberANDA075264
ManufacturerRPK Pharmaceuticals, Inc.
Substance NameTRETINOIN
Strength.25
Strength Unitmg/g
Pharmacy ClassesRetinoid [EPC], Retinoids [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/53002-8101-1





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