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Ortho Micronor
Ortho Micronor - 50458-194-23 - (NORETHINDRONE)
Drug Information of Ortho Micronor
| Product NDC: | 50458-194 |
| Proprietary Name: | Ortho Micronor |
| Non Proprietary Name: | NORETHINDRONE |
| Active Ingredient(s): | .35 mg/1 & nbsp; NORETHINDRONE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ortho Micronor
| Product NDC: | 50458-194 |
| Labeler Name: | Janssen Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016954 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19730102 |
Package Information of Ortho Micronor
| Package NDC: | 50458-194-23 |
| Package Description: | 12 BLISTER PACK in 1 CARTON (50458-194-23) > 28 TABLET in 1 BLISTER PACK (50458-194-00) |
NDC Information of Ortho Micronor
| NDC Code | 50458-194-23 |
| Proprietary Name | Ortho Micronor |
| Package Description | 12 BLISTER PACK in 1 CARTON (50458-194-23) > 28 TABLET in 1 BLISTER PACK (50458-194-00) |
| Product NDC | 50458-194 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | NORETHINDRONE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19730102 |
| Marketing Category Name | NDA |
| Labeler Name | Janssen Pharmaceuticals, Inc. |
| Substance Name | NORETHINDRONE |
| Strength Number | .35 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
