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Tri-Lo-Sprintec - 0093-2140-28 - (norgestimate and ethinyl estradiol)

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Drug Information of Tri-Lo-Sprintec

Product NDC: 0093-2140
Proprietary Name: Tri-Lo-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-Lo-Sprintec

Product NDC: 0093-2140
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076784
Marketing Category: ANDA
Start Marketing Date: 20120703

Package Information of Tri-Lo-Sprintec

Package NDC: 0093-2140-28
Package Description: 6 POUCH in 1 CARTON (0093-2140-28) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK

NDC Information of Tri-Lo-Sprintec

NDC Code 0093-2140-28
Proprietary Name Tri-Lo-Sprintec
Package Description 6 POUCH in 1 CARTON (0093-2140-28) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK
Product NDC 0093-2140
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name norgestimate and ethinyl estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 20120703
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Tri-Lo-Sprintec


General Information