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Endometrin
Endometrin - 55566-6500-3 - (Progesterone)
Drug Information of Endometrin
| Product NDC: | 55566-6500 |
| Proprietary Name: | Endometrin |
| Non Proprietary Name: | Progesterone |
| Active Ingredient(s): | 100 mg/1 & nbsp; Progesterone |
| Administration Route(s): | VAGINAL |
| Dosage Form(s): | INSERT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Endometrin
| Product NDC: | 55566-6500 |
| Labeler Name: | Ferring Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022057 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20070621 |
Package Information of Endometrin
| Package NDC: | 55566-6500-3 |
| Package Description: | 1 CARTON in 1 CARTON (55566-6500-3) > 21 BLISTER PACK in 1 CARTON (55566-6500-2) > 1 INSERT in 1 BLISTER PACK (55566-6500-1) |
NDC Information of Endometrin
| NDC Code | 55566-6500-3 |
| Proprietary Name | Endometrin |
| Package Description | 1 CARTON in 1 CARTON (55566-6500-3) > 21 BLISTER PACK in 1 CARTON (55566-6500-2) > 1 INSERT in 1 BLISTER PACK (55566-6500-1) |
| Product NDC | 55566-6500 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Progesterone |
| Dosage Form Name | INSERT |
| Route Name | VAGINAL |
| Start Marketing Date | 20070621 |
| Marketing Category Name | NDA |
| Labeler Name | Ferring Pharmaceuticals Inc. |
| Substance Name | PROGESTERONE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Progesterone [Chemical/Ingredient],Progesterone [EPC] |
