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Tri-Sprintec - 54868-5028-0 - (norgestimate and ethinyl estradiol)

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Drug Information of Tri-Sprintec

Product NDC: 54868-5028
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: 54868-5028
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075808
Marketing Category: ANDA
Start Marketing Date: 20040326

Package Information of Tri-Sprintec

Package NDC: 54868-5028-0
Package Description: 1 POUCH in 1 CARTON (54868-5028-0) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK

NDC Information of Tri-Sprintec

NDC Code 54868-5028-0
Proprietary Name Tri-Sprintec
Package Description 1 POUCH in 1 CARTON (54868-5028-0) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK
Product NDC 54868-5028
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name norgestimate and ethinyl estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 20040326
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Tri-Sprintec


General Information