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Azurette
Azurette - 52544-940-28 - (Desogestrel/Ethinyl Estradiol and Ethinyl Estradiol)
Drug Information of Azurette
| Product NDC: | 52544-940 |
| Proprietary Name: | Azurette |
| Non Proprietary Name: | Desogestrel/Ethinyl Estradiol and Ethinyl Estradiol |
| Active Ingredient(s): | & nbsp; Desogestrel/Ethinyl Estradiol and Ethinyl Estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Azurette
| Product NDC: | 52544-940 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076916 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081229 |
Package Information of Azurette
| Package NDC: | 52544-940-28 |
| Package Description: | 6 POUCH in 1 CARTON (52544-940-28) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK |
NDC Information of Azurette
| NDC Code | 52544-940-28 |
| Proprietary Name | Azurette |
| Package Description | 6 POUCH in 1 CARTON (52544-940-28) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK |
| Product NDC | 52544-940 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Desogestrel/Ethinyl Estradiol and Ethinyl Estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20081229 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Pharma, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
