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Depo-Provera
Depo-Provera - 0009-7376-01 - (medroxyprogesterone acetate)
Drug Information of Depo-Provera
| Product NDC: | 0009-7376 |
| Proprietary Name: | Depo-Provera |
| Non Proprietary Name: | medroxyprogesterone acetate |
| Active Ingredient(s): | 150 mg/mL & nbsp; medroxyprogesterone acetate |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION, SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Depo-Provera
| Product NDC: | 0009-7376 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020246 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19921029 |
Package Information of Depo-Provera
| Package NDC: | 0009-7376-01 |
| Package Description: | 1 mL in 1 SYRINGE (0009-7376-01) |
NDC Information of Depo-Provera
| NDC Code | 0009-7376-01 |
| Proprietary Name | Depo-Provera |
| Package Description | 1 mL in 1 SYRINGE (0009-7376-01) |
| Product NDC | 0009-7376 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | medroxyprogesterone acetate |
| Dosage Form Name | INJECTION, SUSPENSION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 19921029 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | MEDROXYPROGESTERONE ACETATE |
| Strength Number | 150 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
