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Solia
Solia - 66993-611-28 - (desogestrel and ethinyl estradiol)
Drug Information of Solia
| Product NDC: | 66993-611 |
| Proprietary Name: | Solia |
| 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 Solia
| Product NDC: | 66993-611 |
| Labeler Name: | Prasco Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020071 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20110201 |
Package Information of Solia
| Package NDC: | 66993-611-28 |
| Package Description: | 6 BLISTER PACK in 1 BOX (66993-611-28) > 1 KIT in 1 BLISTER PACK |
NDC Information of Solia
| NDC Code | 66993-611-28 |
| Proprietary Name | Solia |
| Package Description | 6 BLISTER PACK in 1 BOX (66993-611-28) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 66993-611 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | desogestrel and ethinyl estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20110201 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Prasco Laboratories |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
