| Product NDC: | 68462-565 |
| Proprietary Name: | Norgestimate and Ethinyl Estradiol |
| Non Proprietary Name: | Norgestimate and Ethinyl Estradiol |
| Active Ingredient(s): | & nbsp; Norgestimate and Ethinyl Estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68462-565 |
| Labeler Name: | Glenmark Generics Inc., USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200494 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110617 |
| Package NDC: | 68462-565-29 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68462-565-29) > 1 KIT in 1 BLISTER PACK |
| NDC Code | 68462-565-29 |
| Proprietary Name | Norgestimate and Ethinyl Estradiol |
| Package Description | 3 BLISTER PACK in 1 CARTON (68462-565-29) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 68462-565 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Norgestimate and Ethinyl Estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20110617 |
| Marketing Category Name | ANDA |
| Labeler Name | Glenmark Generics Inc., USA |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |