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OVCON 35
OVCON 35 - 0430-0580-14 - (Norethindrone and Ethinyl Estradiol)
Drug Information of OVCON 35
| Product NDC: | 0430-0580 |
| Proprietary Name: | OVCON 35 |
| Non Proprietary Name: | Norethindrone and Ethinyl Estradiol |
| Active Ingredient(s): | & nbsp; Norethindrone and Ethinyl Estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OVCON 35
| Product NDC: | 0430-0580 |
| Labeler Name: | Warner Chilcott (US), LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076238 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050601 |
Package Information of OVCON 35
| Package NDC: | 0430-0580-14 |
| Package Description: | 72 CARTON in 1 CASE (0430-0580-14) > 5 CELLO PACK in 1 CARTON > 1 BLISTER PACK in 1 CELLO PACK > 1 KIT in 1 BLISTER PACK |
NDC Information of OVCON 35
| NDC Code | 0430-0580-14 |
| Proprietary Name | OVCON 35 |
| Package Description | 72 CARTON in 1 CASE (0430-0580-14) > 5 CELLO PACK in 1 CARTON > 1 BLISTER PACK in 1 CELLO PACK > 1 KIT in 1 BLISTER PACK |
| Product NDC | 0430-0580 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Norethindrone and Ethinyl Estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20050601 |
| Marketing Category Name | ANDA |
| Labeler Name | Warner Chilcott (US), LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
