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Tilia Fe
Tilia Fe - 21695-685-28 - (Norethindrone Acetate and Ethinyl Estradiol)
Drug Information of Tilia Fe
| Product NDC: | 21695-685 |
| Proprietary Name: | Tilia 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 Tilia Fe
| Product NDC: | 21695-685 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076629 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101201 |
Package Information of Tilia Fe
| Package NDC: | 21695-685-28 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (21695-685-28) > 1 KIT in 1 BLISTER PACK |
NDC Information of Tilia Fe
| NDC Code | 21695-685-28 |
| Proprietary Name | Tilia Fe |
| Package Description | 3 BLISTER PACK in 1 CARTON (21695-685-28) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 21695-685 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Norethindrone Acetate and Ethinyl Estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20101201 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
