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Desogen
Desogen - 0052-0261-06 - (desogestrel and ethinyl estradiol)
Drug Information of Desogen
| Product NDC: | 0052-0261 |
| Proprietary Name: | Desogen |
| Non Proprietary Name: | desogestrel and ethinyl estradiol |
| Active Ingredient(s): | & nbsp; desogestrel and ethinyl estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Desogen
| Product NDC: | 0052-0261 |
| Labeler Name: | Organon Pharmaceuticals USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020071 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100610 |
Package Information of Desogen
| Package NDC: | 0052-0261-06 |
| Package Description: | 6 BLISTER PACK in 1 BOX (0052-0261-06) > 1 KIT in 1 BLISTER PACK |
NDC Information of Desogen
| NDC Code | 0052-0261-06 |
| Proprietary Name | Desogen |
| Package Description | 6 BLISTER PACK in 1 BOX (0052-0261-06) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 0052-0261 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | desogestrel and ethinyl estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20100610 |
| Marketing Category Name | NDA |
| Labeler Name | Organon Pharmaceuticals USA |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
