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Progesterone
Progesterone - 0143-9725-01 - (Progesterone)
Drug Information of Progesterone
| Product NDC: | 0143-9725 |
| Proprietary Name: | Progesterone |
| Non Proprietary Name: | Progesterone |
| Active Ingredient(s): | 50 mg/1 & nbsp; Progesterone |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Progesterone
| Product NDC: | 0143-9725 |
| Labeler Name: | West-ward Pharmaceutical Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091033 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101028 |
Package Information of Progesterone
| Package NDC: | 0143-9725-01 |
| Package Description: | 10 INJECTION in 1 BOX (0143-9725-01) |
NDC Information of Progesterone
| NDC Code | 0143-9725-01 |
| Proprietary Name | Progesterone |
| Package Description | 10 INJECTION in 1 BOX (0143-9725-01) |
| Product NDC | 0143-9725 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Progesterone |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20101028 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp |
| Substance Name | PROGESTERONE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Progesterone [Chemical/Ingredient],Progesterone [EPC] |
