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Junel Fe 1.5/30
Junel Fe 1.5/30 - 54868-5935-0 - (norethindrone acetate and ethinyl estradiol, and ferrous fumarate)
Drug Information of Junel Fe 1.5/30
| Product NDC: | 54868-5935 |
| Proprietary Name: | Junel Fe 1.5/30 |
| Non Proprietary Name: | norethindrone acetate and ethinyl estradiol, and ferrous fumarate |
| Active Ingredient(s): | & nbsp; norethindrone acetate and ethinyl estradiol, and ferrous fumarate |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Junel Fe 1.5/30
| Product NDC: | 54868-5935 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076064 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080902 |
Package Information of Junel Fe 1.5/30
| Package NDC: | 54868-5935-0 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (54868-5935-0) > 1 KIT in 1 BLISTER PACK |
NDC Information of Junel Fe 1.5/30
| NDC Code | 54868-5935-0 |
| Proprietary Name | Junel Fe 1.5/30 |
| Package Description | 1 BLISTER PACK in 1 CARTON (54868-5935-0) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 54868-5935 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | norethindrone acetate and ethinyl estradiol, and ferrous fumarate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20080902 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
