Product NDC: | 0093-3134 |
Proprietary Name: | CAMRESE |
Non Proprietary Name: | levonorgestrel / ethinyl estradiol and ethinyl estradiol |
Active Ingredient(s): | & nbsp; levonorgestrel / ethinyl estradiol and ethinyl estradiol |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0093-3134 |
Labeler Name: | TEVA Pharmaceuticals USA Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021840 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20100728 |
Package NDC: | 0093-3134-91 |
Package Description: | 1 BLISTER PACK in 1 POUCH (0093-3134-91) > 1 KIT in 1 BLISTER PACK |
NDC Code | 0093-3134-91 |
Proprietary Name | CAMRESE |
Package Description | 1 BLISTER PACK in 1 POUCH (0093-3134-91) > 1 KIT in 1 BLISTER PACK |
Product NDC | 0093-3134 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | levonorgestrel / ethinyl estradiol and ethinyl estradiol |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20100728 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | TEVA Pharmaceuticals USA Inc |
Substance Name | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |