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Osphena
Osphena - 59630-580-30 - (Ospemifene)
Drug Information of Osphena
| Product NDC: | 59630-580 |
| Proprietary Name: | Osphena |
| Non Proprietary Name: | Ospemifene |
| Active Ingredient(s): | 60 mg/1 & nbsp; Ospemifene |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Osphena
| Product NDC: | 59630-580 |
| Labeler Name: | Shionogi Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA203505 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130226 |
Package Information of Osphena
| Package NDC: | 59630-580-30 |
| Package Description: | 2 BLISTER PACK in 1 PACKAGE (59630-580-30) > 15 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Osphena
| NDC Code | 59630-580-30 |
| Proprietary Name | Osphena |
| Package Description | 2 BLISTER PACK in 1 PACKAGE (59630-580-30) > 15 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 59630-580 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ospemifene |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130226 |
| Marketing Category Name | NDA |
| Labeler Name | Shionogi Inc. |
| Substance Name | OSPEMIFENE |
| Strength Number | 60 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
