Home
>
National Drug Code (NDC)
>
CAMRESE
CAMRESE - 0093-3134-91 - (levonorgestrel / ethinyl estradiol and ethinyl estradiol)
Drug Information of CAMRESE
| 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) |
Labeler Information of CAMRESE
| 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 Information of CAMRESE
| Package NDC: | 0093-3134-91 |
| Package Description: | 1 BLISTER PACK in 1 POUCH (0093-3134-91) > 1 KIT in 1 BLISTER PACK |
NDC Information of CAMRESE
| 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 |
