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VIORELE
VIORELE - 68462-318-29 - (Desogestrel and Ethinyl Estradiol and Ethinyl Estradiol)
Drug Information of VIORELE
| Product NDC: | 68462-318 |
| Proprietary Name: | VIORELE |
| Non Proprietary Name: | Desogestrel and Ethinyl Estradiol and Ethinyl Estradiol |
| Active Ingredient(s): | & nbsp; Desogestrel and Ethinyl Estradiol and Ethinyl Estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of VIORELE
| Product NDC: | 68462-318 |
| Labeler Name: | Glenmark Generics Inc., USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091346 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120404 |
Package Information of VIORELE
| Package NDC: | 68462-318-29 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68462-318-29) > 1 KIT in 1 BLISTER PACK |
NDC Information of VIORELE
| NDC Code | 68462-318-29 |
| Proprietary Name | VIORELE |
| Package Description | 3 BLISTER PACK in 1 CARTON (68462-318-29) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 68462-318 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Desogestrel and Ethinyl Estradiol and Ethinyl Estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20120404 |
| Marketing Category Name | ANDA |
| Labeler Name | Glenmark Generics Inc., USA |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
