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Tri-Sprintec
Tri-Sprintec - 21695-770-01 - (norgestimate and ethinyl estradiol)
Drug Information of Tri-Sprintec
| Product NDC: | 21695-770 |
| Proprietary Name: | Tri-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 Tri-Sprintec
| Product NDC: | 21695-770 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075808 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110125 |
Package Information of Tri-Sprintec
| Package NDC: | 21695-770-01 |
| Package Description: | 1 BLISTER PACK in 1 POUCH (21695-770-01) > 1 KIT in 1 BLISTER PACK |
NDC Information of Tri-Sprintec
| NDC Code | 21695-770-01 |
| Proprietary Name | Tri-Sprintec |
| Package Description | 1 BLISTER PACK in 1 POUCH (21695-770-01) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 21695-770 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | norgestimate and ethinyl estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20110125 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
