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Prefest - 51285-063-90 - (estradiol/norgestimate)
Drug Information of Prefest
| Product NDC: | 51285-063 |
| Proprietary Name: | Prefest |
| Non Proprietary Name: | estradiol/norgestimate |
| Active Ingredient(s): | & nbsp; estradiol/norgestimate |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Prefest
| Product NDC: | 51285-063 |
| Labeler Name: | Teva Women's Health, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076812 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060530 |
Package Information of Prefest
| Package NDC: | 51285-063-90 |
| Package Description: | 6 POUCH in 1 CARTON (51285-063-90) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK |
NDC Information of Prefest
| NDC Code | 51285-063-90 |
| Proprietary Name | Prefest |
| Package Description | 6 POUCH in 1 CARTON (51285-063-90) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK |
| Product NDC | 51285-063 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | estradiol/norgestimate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20060530 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Women's Health, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
