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Progesterone
Progesterone - 0517-0750-01 - (Progesterone)
Drug Information of Progesterone
| Product NDC: | 0517-0750 |
| Proprietary Name: | Progesterone |
| Non Proprietary Name: | Progesterone |
| Active Ingredient(s): | 50 mg/mL & nbsp; Progesterone |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Progesterone
| Product NDC: | 0517-0750 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090845 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100929 |
Package Information of Progesterone
| Package NDC: | 0517-0750-01 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (0517-0750-01) > 10 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Progesterone
| NDC Code | 0517-0750-01 |
| Proprietary Name | Progesterone |
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0517-0750-01) > 10 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 0517-0750 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Progesterone |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20100929 |
| Marketing Category Name | ANDA |
| Labeler Name | American Regent, Inc. |
| Substance Name | PROGESTERONE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Progesterone [Chemical/Ingredient],Progesterone [EPC] |
