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Vivelle Dot - 0078-0344-45 - (estradiol)

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Drug Information of Vivelle Dot

Product NDC: 0078-0344
Proprietary Name: Vivelle Dot
Non Proprietary Name: estradiol
Active Ingredient(s): .05    mg/d & nbsp;   estradiol
Administration Route(s): TRANSDERMAL
Dosage Form(s): PATCH, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Vivelle Dot

Product NDC: 0078-0344
Labeler Name: Novartis Pharmaceuticals Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020538
Marketing Category: NDA
Start Marketing Date: 19990108

Package Information of Vivelle Dot

Package NDC: 0078-0344-45
Package Description: 3 PACKET in 1 CARTON (0078-0344-45) > 8 POUCH in 1 PACKET (0078-0344-42) > 1 PATCH in 1 POUCH (0078-0344-62) > 3.5 d in 1 PATCH

NDC Information of Vivelle Dot

NDC Code 0078-0344-45
Proprietary Name Vivelle Dot
Package Description 3 PACKET in 1 CARTON (0078-0344-45) > 8 POUCH in 1 PACKET (0078-0344-42) > 1 PATCH in 1 POUCH (0078-0344-62) > 3.5 d in 1 PATCH
Product NDC 0078-0344
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name estradiol
Dosage Form Name PATCH, EXTENDED RELEASE
Route Name TRANSDERMAL
Start Marketing Date 19990108
Marketing Category Name NDA
Labeler Name Novartis Pharmaceuticals Corporation
Substance Name ESTRADIOL
Strength Number .05
Strength Unit mg/d
Pharmaceutical Classes Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA]

Complete Information of Vivelle Dot


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