Product NDC: | 66116-436 |
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) |
Product NDC: | 66116-436 |
Labeler Name: | MedVantx, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075808 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110125 |
Package NDC: | 66116-436-28 |
Package Description: | 1 POUCH in 1 CARTON (66116-436-28) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK |
NDC Code | 66116-436-28 |
Proprietary Name | Tri-Sprintec |
Package Description | 1 POUCH in 1 CARTON (66116-436-28) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK |
Product NDC | 66116-436 |
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 | MedVantx, Inc. |
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