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Tilia Fe
Tilia Fe - 54868-6274-0 - (Norethindrone Acetate and Ethinyl Estradiol)
Drug Information of Tilia Fe
| Product NDC: | 54868-6274 |
| Proprietary Name: | Tilia Fe |
| Non Proprietary Name: | Norethindrone Acetate and Ethinyl Estradiol |
| Active Ingredient(s): | & nbsp; Norethindrone Acetate and Ethinyl Estradiol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tilia Fe
| Product NDC: | 54868-6274 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076629 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110621 |
Package Information of Tilia Fe
| Package NDC: | 54868-6274-0 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (54868-6274-0) > 1 KIT in 1 BLISTER PACK |
NDC Information of Tilia Fe
| NDC Code | 54868-6274-0 |
| Proprietary Name | Tilia Fe |
| Package Description | 1 BLISTER PACK in 1 CARTON (54868-6274-0) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 54868-6274 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Norethindrone Acetate and Ethinyl Estradiol |
| Dosage Form Name | KIT |
| Route Name | ORAL |
| Start Marketing Date | 20110621 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
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