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Microgestin
Microgestin - 52544-950-21 - (Norethindrone Acetate and Ethinyl Estradiol)
Drug Information of Microgestin
| Product NDC: | 52544-950 |
| Proprietary Name: | Microgestin |
| Non Proprietary Name: | Norethindrone Acetate and Ethinyl Estradiol |
| Active Ingredient(s): | .02; 1 mg/1; mg/1 & nbsp; Norethindrone Acetate and Ethinyl Estradiol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Microgestin
| Product NDC: | 52544-950 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075647 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010205 |
Package Information of Microgestin
| Package NDC: | 52544-950-21 |
| Package Description: | 6 BLISTER PACK in 1 CARTON (52544-950-21) > 21 TABLET in 1 BLISTER PACK |
NDC Information of Microgestin
| NDC Code | 52544-950-21 |
| Proprietary Name | Microgestin |
| Package Description | 6 BLISTER PACK in 1 CARTON (52544-950-21) > 21 TABLET in 1 BLISTER PACK |
| Product NDC | 52544-950 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Norethindrone Acetate and Ethinyl Estradiol |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20010205 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Pharma, Inc. |
| Substance Name | ETHINYL ESTRADIOL; NORETHINDRONE ACETATE |
| Strength Number | .02; 1 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |
