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Prochieve
Prochieve - 55056-1601-8 - (progesterone)
Drug Information of Prochieve
| Product NDC: | 55056-1601 |
| Proprietary Name: | Prochieve |
| Non Proprietary Name: | progesterone |
| Active Ingredient(s): | 90 mg/1.125g & nbsp; progesterone |
| Administration Route(s): | VAGINAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Prochieve
| Product NDC: | 55056-1601 |
| Labeler Name: | Columbia Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020701 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19970513 |
Package Information of Prochieve
| Package NDC: | 55056-1601-8 |
| Package Description: | 18 APPLICATOR in 1 CARTON (55056-1601-8) > 1.125 g in 1 APPLICATOR |
NDC Information of Prochieve
| NDC Code | 55056-1601-8 |
| Proprietary Name | Prochieve |
| Package Description | 18 APPLICATOR in 1 CARTON (55056-1601-8) > 1.125 g in 1 APPLICATOR |
| Product NDC | 55056-1601 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | progesterone |
| Dosage Form Name | GEL |
| Route Name | VAGINAL |
| Start Marketing Date | 19970513 |
| Marketing Category Name | NDA |
| Labeler Name | Columbia Laboratories |
| Substance Name | PROGESTERONE |
| Strength Number | 90 |
| Strength Unit | mg/1.125g |
| Pharmaceutical Classes | Progesterone [Chemical/Ingredient],Progesterone [EPC] |
