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Tri-Legest Fe
Tri-Legest Fe - 0555-9032-70 - (Norethindrone Acetate and Ethinyl Estradiol)
Drug Information of Tri-Legest Fe
| Product NDC: | 0555-9032 |
| Proprietary Name: | Tri-Legest Fe |
| Non Proprietary Name: | Norethindrone Acetate and Ethinyl Estradiol |
| Active Ingredient(s): | & nbsp; Norethindrone Acetate and Ethinyl Estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tri-Legest Fe
| Product NDC: | 0555-9032 |
| Labeler Name: | Barr Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076105 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20071026 |
Package Information of Tri-Legest Fe
| Package NDC: | 0555-9032-70 |
| Package Description: | 5 BLISTER PACK in 1 CARTON (0555-9032-70) > 1 KIT in 1 BLISTER PACK |
NDC Information of Tri-Legest Fe
| NDC Code | 0555-9032-70 |
| Proprietary Name | Tri-Legest Fe |
| Package Description | 5 BLISTER PACK in 1 CARTON (0555-9032-70) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 0555-9032 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Norethindrone Acetate and Ethinyl Estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20071026 |
| Marketing Category Name | ANDA |
| Labeler Name | Barr Laboratories Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
