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Medroxyprogesterone Acetate
Medroxyprogesterone Acetate - 0703-6801-04 - (medroxyprogesterone acetate)
Drug Information of Medroxyprogesterone Acetate
| Product NDC: | 0703-6801 |
| Proprietary Name: | Medroxyprogesterone Acetate |
| Non Proprietary Name: | medroxyprogesterone acetate |
| Active Ingredient(s): | 150 mg/mL & nbsp; medroxyprogesterone acetate |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Medroxyprogesterone Acetate
| Product NDC: | 0703-6801 |
| Labeler Name: | Teva Parenteral Medicines, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076553 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040914 |
Package Information of Medroxyprogesterone Acetate
| Package NDC: | 0703-6801-04 |
| Package Description: | 25 VIAL in 1 TRAY (0703-6801-04) > 1 mL in 1 VIAL |
NDC Information of Medroxyprogesterone Acetate
| NDC Code | 0703-6801-04 |
| Proprietary Name | Medroxyprogesterone Acetate |
| Package Description | 25 VIAL in 1 TRAY (0703-6801-04) > 1 mL in 1 VIAL |
| Product NDC | 0703-6801 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | medroxyprogesterone acetate |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20040914 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Parenteral Medicines, Inc |
| Substance Name | MEDROXYPROGESTERONE ACETATE |
| Strength Number | 150 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
