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Modicon
Modicon - 50458-171-15 - (norethindrone and ethinyl estradiol)
Drug Information of Modicon
| Product NDC: | 50458-171 |
| Proprietary Name: | Modicon |
| 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 Modicon
| Product NDC: | 50458-171 |
| Labeler Name: | Janssen Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018985 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19840404 |
Package Information of Modicon
| Package NDC: | 50458-171-15 |
| Package Description: | 6 DIALPACK in 1 CARTON (50458-171-15) > 1 KIT in 1 DIALPACK (50458-171-00) |
NDC Information of Modicon
| NDC Code | 50458-171-15 |
| Proprietary Name | Modicon |
| Package Description | 6 DIALPACK in 1 CARTON (50458-171-15) > 1 KIT in 1 DIALPACK (50458-171-00) |
| Product NDC | 50458-171 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | norethindrone and ethinyl estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19840404 |
| Marketing Category Name | NDA |
| Labeler Name | Janssen Pharmaceuticals, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
