"0046-1105-51" National Drug Code (NDC)

Prempro 1 POUCH in 1 CARTON (0046-1105-51) > 1 BLISTER PACK in 1 POUCH > 5 TABLET, SUGAR COATED in 1 BLISTER PACK
(Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.)

NDC Code0046-1105-51
Package Description1 POUCH in 1 CARTON (0046-1105-51) > 1 BLISTER PACK in 1 POUCH > 5 TABLET, SUGAR COATED in 1 BLISTER PACK
Product NDC0046-1105
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrempro
Non-Proprietary NameConjugated Estrogens And Medroxyprogesterone Acetate
Dosage FormTABLET, SUGAR COATED
UsageORAL
Start Marketing Date20090921
Marketing Category NameNDA
Application NumberNDA020527
ManufacturerWyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.
Substance NameESTROGENS, CONJUGATED; MEDROXYPROGESTERONE ACETATE
Strength.3; 1.5
Strength Unitmg/1; mg/1
Pharmacy ClassesEstrogen [EPC],Estrogen Receptor Agonists [MoA],Estrogens, Conjugated (USP) [Chemical/Ingredient],Progesterone Congeners [Chemical/Ingredient],Progestin [EPC]

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