methazolamide
METHAZOLAMIDE TABLETS USP 25 mg and 50 mg Rx Only
Approved
Approval ID
8395cda9-1a6d-408c-8818-4a5d90c4a4e0
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 18, 2020
Manufacturers
FDA
A-S Medication Solutions
DUNS: 830016429
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
methazolamide
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code50090-3233
Application NumberANDA040062
Product Classification
M
Marketing Category
C73584
G
Generic Name
methazolamide
Product Specifications
Route of AdministrationORAL
Effective DateNovember 12, 2018
FDA Product Classification
INGREDIENTS (6)
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
METHAZOLAMIDEActive
Quantity: 50 mg in 1 1
Code: W733B0S9SD
Classification: ACTIB
DIBASIC CALCIUM PHOSPHATE DIHYDRATEInactive
Code: O7TSZ97GEP
Classification: IACT
MICROCRYSTALLINE CELLULOSEInactive
Code: OP1R32D61U
Classification: IACT