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TriNessa
TriNessa - 21695-407-01 - (Norgestimate and Ethinyl Estradiol)
Drug Information of TriNessa
| Product NDC: | 21695-407 |
| Proprietary Name: | TriNessa |
| 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 TriNessa
| Product NDC: | 21695-407 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019697 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20070817 |
Package Information of TriNessa
| Package NDC: | 21695-407-01 |
| Package Description: | 6 DIALPACK in 1 CARTON (21695-407-01) > 1 KIT in 1 DIALPACK |
NDC Information of TriNessa
| NDC Code | 21695-407-01 |
| Proprietary Name | TriNessa |
| Package Description | 6 DIALPACK in 1 CARTON (21695-407-01) > 1 KIT in 1 DIALPACK |
| Product NDC | 21695-407 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Norgestimate and Ethinyl Estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20070817 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
