Product NDC: | 52544-554 |
Proprietary Name: | Necon 10/11 |
Non Proprietary Name: | Norethindrone and Ethinyl Estradiol Tablets |
Active Ingredient(s): | & nbsp; Norethindrone and Ethinyl Estradiol Tablets |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52544-554 |
Labeler Name: | Watson Pharma, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA071044 |
Marketing Category: | ANDA |
Start Marketing Date: | 19880401 |
Package NDC: | 52544-554-28 |
Package Description: | 6 BLISTER PACK in 1 CARTON (52544-554-28) > 1 KIT in 1 BLISTER PACK |
NDC Code | 52544-554-28 |
Proprietary Name | Necon 10/11 |
Package Description | 6 BLISTER PACK in 1 CARTON (52544-554-28) > 1 KIT in 1 BLISTER PACK |
Product NDC | 52544-554 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Norethindrone and Ethinyl Estradiol Tablets |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 19880401 |
Marketing Category Name | ANDA |
Labeler Name | Watson Pharma, Inc. |
Substance Name | |
Strength Number | |
Strength Unit | |
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