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Femring
Femring - 0430-6202-40 - (estradiol acetate)
Drug Information of Femring
| Product NDC: | 0430-6202 |
| Proprietary Name: | Femring |
| Non Proprietary Name: | estradiol acetate |
| Active Ingredient(s): | .1 mg/d & nbsp; estradiol acetate |
| Administration Route(s): | VAGINAL |
| Dosage Form(s): | RING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Femring
| Product NDC: | 0430-6202 |
| Labeler Name: | Warner Chilcott (US), LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021367 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030701 |
Package Information of Femring
| Package NDC: | 0430-6202-40 |
| Package Description: | 12 CARTON in 1 CASE (0430-6202-40) > 1 POUCH in 1 CARTON > 90 d in 1 POUCH |
NDC Information of Femring
| NDC Code | 0430-6202-40 |
| Proprietary Name | Femring |
| Package Description | 12 CARTON in 1 CASE (0430-6202-40) > 1 POUCH in 1 CARTON > 90 d in 1 POUCH |
| Product NDC | 0430-6202 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | estradiol acetate |
| Dosage Form Name | RING |
| Route Name | VAGINAL |
| Start Marketing Date | 20030701 |
| Marketing Category Name | NDA |
| Labeler Name | Warner Chilcott (US), LLC |
| Substance Name | ESTRADIOL ACETATE |
| Strength Number | .1 |
| Strength Unit | mg/d |
| Pharmaceutical Classes | Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |
