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Aranelle
Aranelle - 0555-9066-67 - (norethindrone and ethinyl estradiol)
Drug Information of Aranelle
| Product NDC: | 0555-9066 |
| Proprietary Name: | Aranelle |
| Non Proprietary Name: | norethindrone and ethinyl estradiol |
| Active Ingredient(s): | & nbsp; norethindrone and ethinyl estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aranelle
| Product NDC: | 0555-9066 |
| Labeler Name: | Barr Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076783 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20041004 |
Package Information of Aranelle
| Package NDC: | 0555-9066-67 |
| Package Description: | 3 POUCH in 1 CARTON (0555-9066-67) > 28 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK |
NDC Information of Aranelle
| NDC Code | 0555-9066-67 |
| Proprietary Name | Aranelle |
| Package Description | 3 POUCH in 1 CARTON (0555-9066-67) > 28 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK |
| Product NDC | 0555-9066 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | norethindrone and ethinyl estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20041004 |
| Marketing Category Name | ANDA |
| Labeler Name | Barr Laboratories Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
