 
                        | 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] |