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Levonorgestrel - 45802-840-54 - (Levonorgestrel)

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Drug Information of Levonorgestrel

Product NDC: 45802-840
Proprietary Name: Levonorgestrel
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 Levonorgestrel

Product NDC: 45802-840
Labeler Name: Perrigo New York Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090740
Marketing Category: ANDA
Start Marketing Date: 20110310

Package Information of Levonorgestrel

Package NDC: 45802-840-54
Package Description: 1 BLISTER PACK in 1 CARTON (45802-840-54) > 2 TABLET in 1 BLISTER PACK

NDC Information of Levonorgestrel

NDC Code 45802-840-54
Proprietary Name Levonorgestrel
Package Description 1 BLISTER PACK in 1 CARTON (45802-840-54) > 2 TABLET in 1 BLISTER PACK
Product NDC 45802-840
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levonorgestrel
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110310
Marketing Category Name ANDA
Labeler Name Perrigo New York 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 Levonorgestrel


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