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Progesterone
Progesterone - 63323-261-10 - (PROGESTERONE)
Drug Information of Progesterone
| Product NDC: | 63323-261 |
| 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: | 63323-261 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075906 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010719 |
Package Information of Progesterone
| Package NDC: | 63323-261-10 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (63323-261-10) > 10 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Progesterone
| NDC Code | 63323-261-10 |
| Proprietary Name | Progesterone |
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (63323-261-10) > 10 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 63323-261 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PROGESTERONE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20010719 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | PROGESTERONE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Progesterone [Chemical/Ingredient],Progesterone [EPC] |
