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Prometrium
Prometrium - 0032-1711-01 - (Progesterone)
Drug Information of Prometrium
| Product NDC: | 0032-1711 |
| Proprietary Name: | Prometrium |
| Non Proprietary Name: | Progesterone |
| Active Ingredient(s): | 200 mg/1 & nbsp; Progesterone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Prometrium
| Product NDC: | 0032-1711 |
| Labeler Name: | Abbott Products, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019781 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100730 |
Package Information of Prometrium
| Package NDC: | 0032-1711-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (0032-1711-01) |
NDC Information of Prometrium
| NDC Code | 0032-1711-01 |
| Proprietary Name | Prometrium |
| Package Description | 100 CAPSULE in 1 BOTTLE (0032-1711-01) |
| Product NDC | 0032-1711 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Progesterone |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20100730 |
| Marketing Category Name | NDA |
| Labeler Name | Abbott Products, Inc. |
| Substance Name | PROGESTERONE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Progesterone [Chemical/Ingredient],Progesterone [EPC] |
