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Microgestin Fe
Microgestin Fe - 52544-631-31 - (Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate)
Drug Information of Microgestin Fe
| Product NDC: | 52544-631 |
| Proprietary Name: | Microgestin Fe |
| Non Proprietary Name: | Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate |
| Active Ingredient(s): | & nbsp; Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Microgestin Fe
| Product NDC: | 52544-631 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075548 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010205 |
Package Information of Microgestin Fe
| Package NDC: | 52544-631-31 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (52544-631-31) > 1 KIT in 1 BLISTER PACK |
NDC Information of Microgestin Fe
| NDC Code | 52544-631-31 |
| Proprietary Name | Microgestin Fe |
| Package Description | 3 BLISTER PACK in 1 CARTON (52544-631-31) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 52544-631 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20010205 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Pharma, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
