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Nordette
Nordette - 51285-091-58 - (Levonorgestrel and Ethinyl Estradiol)
Drug Information of Nordette
| Product NDC: | 51285-091 |
| Proprietary Name: | Nordette |
| Non Proprietary Name: | Levonorgestrel and Ethinyl Estradiol |
| Active Ingredient(s): | & nbsp; Levonorgestrel and Ethinyl Estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nordette
| Product NDC: | 51285-091 |
| Labeler Name: | Teva Women's Health, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018782 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19820721 |
Package Information of Nordette
| Package NDC: | 51285-091-58 |
| Package Description: | 6 BLISTER PACK in 1 CARTON (51285-091-58) > 1 KIT in 1 BLISTER PACK |
NDC Information of Nordette
| NDC Code | 51285-091-58 |
| Proprietary Name | Nordette |
| Package Description | 6 BLISTER PACK in 1 CARTON (51285-091-58) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 51285-091 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levonorgestrel and Ethinyl Estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19820721 |
| Marketing Category Name | NDA |
| Labeler Name | Teva Women's Health, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
