Product NDC: | 68462-309 |
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: | 68462-309 |
Labeler Name: | Glenmark Generics Inc., USA |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA200538 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120406 |
Package NDC: | 68462-309-29 |
Package Description: | 3 BLISTER PACK in 1 CARTON (68462-309-29) > 1 KIT in 1 BLISTER PACK (68462-309-84) |
NDC Code | 68462-309-29 |
Proprietary Name | Norgestimate and Ethinyl Estradiol |
Package Description | 3 BLISTER PACK in 1 CARTON (68462-309-29) > 1 KIT in 1 BLISTER PACK (68462-309-84) |
Product NDC | 68462-309 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Norgestimate and Ethinyl Estradiol |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20120406 |
Marketing Category Name | ANDA |
Labeler Name | Glenmark Generics Inc., USA |
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