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Norgestrel/Ethinyl Estradiol
Norgestrel/Ethinyl Estradiol - 24090-961-84 - (norgestrel/ethinyl estradiol)
Drug Information of Norgestrel/Ethinyl Estradiol
| Product NDC: | 24090-961 |
| Proprietary Name: | Norgestrel/Ethinyl Estradiol |
| Non Proprietary Name: | norgestrel/ethinyl estradiol |
| Active Ingredient(s): | & nbsp; norgestrel/ethinyl estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Norgestrel/Ethinyl Estradiol
| Product NDC: | 24090-961 |
| Labeler Name: | Akrimax Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017802 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19760301 |
Package Information of Norgestrel/Ethinyl Estradiol
| Package NDC: | 24090-961-84 |
| Package Description: | 6 BLISTER PACK in 1 CARTON (24090-961-84) > 1 KIT in 1 BLISTER PACK |
NDC Information of Norgestrel/Ethinyl Estradiol
| NDC Code | 24090-961-84 |
| Proprietary Name | Norgestrel/Ethinyl Estradiol |
| Package Description | 6 BLISTER PACK in 1 CARTON (24090-961-84) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 24090-961 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | norgestrel/ethinyl estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19760301 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Akrimax Pharmaceuticals, LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
