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medroxyprogesterone acetate
medroxyprogesterone acetate - 68084-553-21 - (medroxyprogesterone acetate)
Drug Information of medroxyprogesterone acetate
| Product NDC: | 68084-553 |
| Proprietary Name: | medroxyprogesterone acetate |
| Non Proprietary Name: | medroxyprogesterone acetate |
| Active Ingredient(s): | 2.5 mg/1 & nbsp; medroxyprogesterone acetate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of medroxyprogesterone acetate
| Product NDC: | 68084-553 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA011839 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20120127 |
Package Information of medroxyprogesterone acetate
| Package NDC: | 68084-553-21 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68084-553-21) > 10 TABLET in 1 BLISTER PACK (68084-553-11) |
NDC Information of medroxyprogesterone acetate
| NDC Code | 68084-553-21 |
| Proprietary Name | medroxyprogesterone acetate |
| Package Description | 3 BLISTER PACK in 1 CARTON (68084-553-21) > 10 TABLET in 1 BLISTER PACK (68084-553-11) |
| Product NDC | 68084-553 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | medroxyprogesterone acetate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120127 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | American Health Packaging |
| Substance Name | MEDROXYPROGESTERONE ACETATE |
| Strength Number | 2.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
