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QUARTETTE
QUARTETTE - 51285-431-82 - (levonorgestrel/ethinyl estradiol tablets and ethinyl estradiol tablets)
Drug Information of QUARTETTE
| Product NDC: | 51285-431 |
| Proprietary Name: | QUARTETTE |
| Non Proprietary Name: | levonorgestrel/ethinyl estradiol tablets and ethinyl estradiol tablets |
| Active Ingredient(s): | & nbsp; levonorgestrel/ethinyl estradiol tablets and ethinyl estradiol tablets |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of QUARTETTE
| Product NDC: | 51285-431 |
| Labeler Name: | Teva Women's Health, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA204061 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130329 |
Package Information of QUARTETTE
| Package NDC: | 51285-431-82 |
| Package Description: | 1 POUCH in 1 CARTON (51285-431-82) > 1 KIT in 1 POUCH |
NDC Information of QUARTETTE
| NDC Code | 51285-431-82 |
| Proprietary Name | QUARTETTE |
| Package Description | 1 POUCH in 1 CARTON (51285-431-82) > 1 KIT in 1 POUCH |
| Product NDC | 51285-431 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | levonorgestrel/ethinyl estradiol tablets and ethinyl estradiol tablets |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20130329 |
| Marketing Category Name | NDA |
| Labeler Name | Teva Women's Health, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
