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NEXT CHOICE - 52544-475-36 - (levonorgestrel)

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Drug Information of NEXT CHOICE

Product NDC: 52544-475
Proprietary Name: NEXT CHOICE
Non Proprietary Name: levonorgestrel
Active Ingredient(s): .75    mg/1 & nbsp;   levonorgestrel
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of NEXT CHOICE

Product NDC: 52544-475
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078666
Marketing Category: ANDA
Start Marketing Date: 20090721

Package Information of NEXT CHOICE

Package NDC: 52544-475-36
Package Description: 1 BLISTER PACK in 1 CARTON (52544-475-36) > 2 TABLET in 1 BLISTER PACK

NDC Information of NEXT CHOICE

NDC Code 52544-475-36
Proprietary Name NEXT CHOICE
Package Description 1 BLISTER PACK in 1 CARTON (52544-475-36) > 2 TABLET in 1 BLISTER PACK
Product NDC 52544-475
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levonorgestrel
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090721
Marketing Category Name ANDA
Labeler Name Watson Pharma, Inc.
Substance Name LEVONORGESTREL
Strength Number .75
Strength Unit mg/1
Pharmaceutical Classes Inhibit Ovum Fertilization [PE],Progesterone Congeners [Chemical/Ingredient],Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Progestin-containing Intrauterine Device [EPC]

Complete Information of NEXT CHOICE


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