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Climara Pro - 50419-491-04 - (Estradiol and Levonorgestrel)

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Drug Information of Climara Pro

Product NDC: 50419-491
Proprietary Name: Climara Pro
Non Proprietary Name: Estradiol and Levonorgestrel
Active Ingredient(s): 4.4; 1.39    mg/1; mg/1 & nbsp;   Estradiol and Levonorgestrel
Administration Route(s): TRANSDERMAL
Dosage Form(s): PATCH
Coding System: National Drug Codes(NDC)

Labeler Information of Climara Pro

Product NDC: 50419-491
Labeler Name: Bayer HealthCare Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021258
Marketing Category: NDA
Start Marketing Date: 20050622

Package Information of Climara Pro

Package NDC: 50419-491-04
Package Description: 4 PATCH in 1 CARTON (50419-491-04)

NDC Information of Climara Pro

NDC Code 50419-491-04
Proprietary Name Climara Pro
Package Description 4 PATCH in 1 CARTON (50419-491-04)
Product NDC 50419-491
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Estradiol and Levonorgestrel
Dosage Form Name PATCH
Route Name TRANSDERMAL
Start Marketing Date 20050622
Marketing Category Name NDA
Labeler Name Bayer HealthCare Pharmaceuticals Inc.
Substance Name ESTRADIOL; LEVONORGESTREL
Strength Number 4.4; 1.39
Strength Unit mg/1; mg/1
Pharmaceutical Classes Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA],Inhibit Ovum Fertilization [PE],Progesterone Congeners [Chemical/Ingredient],Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Progestin-containing Intrauterine Device [EPC]

Complete Information of Climara Pro


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