Solodyn - 99207-460-10 - (minocycline hydrochloride)

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Drug Information of Solodyn

Product NDC: 99207-460
Proprietary Name: Solodyn
Non Proprietary Name: minocycline hydrochloride
Active Ingredient(s): 45    mg/1 & nbsp;   minocycline hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Solodyn

Product NDC: 99207-460
Labeler Name: Medicis Pharmaceutical Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050808
Marketing Category: NDA
Start Marketing Date: 20060508

Package Information of Solodyn

Package NDC: 99207-460-10
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (99207-460-10)

NDC Information of Solodyn

NDC Code 99207-460-10
Proprietary Name Solodyn
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (99207-460-10)
Product NDC 99207-460
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name minocycline hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20060508
Marketing Category Name NDA
Labeler Name Medicis Pharmaceutical Corp.
Substance Name MINOCYCLINE HYDROCHLORIDE
Strength Number 45
Strength Unit mg/1
Pharmaceutical Classes Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient]

Complete Information of Solodyn


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