| Product NDC: | 55154-0216 | 
| Proprietary Name: | Premarin | 
| Non Proprietary Name: | conjugated estrogens | 
| Active Ingredient(s): | .625 mg/1 & nbsp; conjugated estrogens | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET, FILM COATED | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 55154-0216 | 
| Labeler Name: | Cardinal Health | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | NDA004782 | 
| Marketing Category: | NDA | 
| Start Marketing Date: | 20060101 | 
| Package NDC: | 55154-0216-0 | 
| Package Description: | 10 POUCH in 1 BAG (55154-0216-0) > 1 TABLET, FILM COATED in 1 POUCH | 
| NDC Code | 55154-0216-0 | 
| Proprietary Name | Premarin | 
| Package Description | 10 POUCH in 1 BAG (55154-0216-0) > 1 TABLET, FILM COATED in 1 POUCH | 
| Product NDC | 55154-0216 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | conjugated estrogens | 
| Dosage Form Name | TABLET, FILM COATED | 
| Route Name | ORAL | 
| Start Marketing Date | 20060101 | 
| Marketing Category Name | NDA | 
| Labeler Name | Cardinal Health | 
| Substance Name | ESTROGENS, CONJUGATED | 
| Strength Number | .625 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes | Estrogen [EPC],Estrogen Receptor Agonists [MoA],Estrogens, Conjugated (USP) [Chemical/Ingredient] |