| Product NDC: | 54868-4369 |
| Proprietary Name: | 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) |
| Product NDC: | 54868-4369 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016954 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030917 |
| Package NDC: | 54868-4369-0 |
| Package Description: | 1 DIALPACK in 1 PACKAGE (54868-4369-0) > 28 TABLET in 1 DIALPACK |
| NDC Code | 54868-4369-0 |
| Proprietary Name | MICRONOR |
| Package Description | 1 DIALPACK in 1 PACKAGE (54868-4369-0) > 28 TABLET in 1 DIALPACK |
| Product NDC | 54868-4369 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | norethindrone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20030917 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | NORETHINDRONE |
| Strength Number | .35 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |