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Progesterone Injection
Progesterone Injection - 40042-050-10 - (Progesterone Injection)
Drug Information of Progesterone Injection
| Product NDC: | 40042-050 |
| Proprietary Name: | Progesterone Injection |
| Non Proprietary Name: | Progesterone Injection |
| Active Ingredient(s): | 50 mg/mL & nbsp; Progesterone Injection |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Progesterone Injection
| Product NDC: | 40042-050 |
| Labeler Name: | PharmaForce, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090845 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090904 |
Package Information of Progesterone Injection
| Package NDC: | 40042-050-10 |
| Package Description: | 10 mL in 1 VIAL, MULTI-DOSE (40042-050-10) |
NDC Information of Progesterone Injection
| NDC Code | 40042-050-10 |
| Proprietary Name | Progesterone Injection |
| Package Description | 10 mL in 1 VIAL, MULTI-DOSE (40042-050-10) |
| Product NDC | 40042-050 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Progesterone Injection |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20090904 |
| Marketing Category Name | ANDA |
| Labeler Name | PharmaForce, Inc. |
| Substance Name | PROGESTERONE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Progesterone [Chemical/Ingredient],Progesterone [EPC] |
