| Product NDC: | 0555-9050 | 
| Proprietary Name: | Kariva | 
| Non Proprietary Name: | desogestrel/ethinyl estradiol and ethinyl estradiol | 
| Active Ingredient(s): | & nbsp; desogestrel/ethinyl estradiol and ethinyl estradiol | 
| Administration Route(s): | |
| Dosage Form(s): | KIT | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 0555-9050 | 
| Labeler Name: | Barr Laboratories Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA075863 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20020408 | 
| Package NDC: | 0555-9050-58 | 
| Package Description: | 6 POUCH in 1 CARTON (0555-9050-58) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK | 
| NDC Code | 0555-9050-58 | 
| Proprietary Name | Kariva | 
| Package Description | 6 POUCH in 1 CARTON (0555-9050-58) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK | 
| Product NDC | 0555-9050 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | desogestrel/ethinyl estradiol and ethinyl estradiol | 
| Dosage Form Name | KIT | 
| Route Name | |
| Start Marketing Date | 20020408 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Barr Laboratories Inc. | 
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |