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Sprintec
Sprintec - 21695-769-28 - (Norgestimate and Ethinyl Estradiol)
Drug Information of Sprintec
| Product NDC: | 21695-769 |
| Proprietary Name: | Sprintec |
| Non Proprietary Name: | Norgestimate and Ethinyl Estradiol |
| Active Ingredient(s): | & nbsp; Norgestimate and Ethinyl Estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sprintec
| Product NDC: | 21695-769 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075804 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101122 |
Package Information of Sprintec
| Package NDC: | 21695-769-28 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (21695-769-28) > 1 KIT in 1 BLISTER PACK |
NDC Information of Sprintec
| NDC Code | 21695-769-28 |
| Proprietary Name | Sprintec |
| Package Description | 1 BLISTER PACK in 1 CARTON (21695-769-28) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 21695-769 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Norgestimate and Ethinyl Estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20101122 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
