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LOESTRIN Fe 1/20
LOESTRIN Fe 1/20 - 51285-080-70 - (norethindrone acetate and ethinyl estradiol and ferrous fumarate)
Drug Information of LOESTRIN Fe 1/20
| Product NDC: | 51285-080 |
| Proprietary Name: | LOESTRIN Fe 1/20 |
| 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 LOESTRIN Fe 1/20
| Product NDC: | 51285-080 |
| Labeler Name: | Teva Women's Health, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076081 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081001 |
Package Information of LOESTRIN Fe 1/20
| Package NDC: | 51285-080-70 |
| Package Description: | 5 POUCH in 1 CARTON (51285-080-70) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK |
NDC Information of LOESTRIN Fe 1/20
| NDC Code | 51285-080-70 |
| Proprietary Name | LOESTRIN Fe 1/20 |
| Package Description | 5 POUCH in 1 CARTON (51285-080-70) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK |
| Product NDC | 51285-080 |
| 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 | 20081001 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Women's Health, Inc |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
