Methazolamide
Methazolamide Tablets USP Rx only
Approved
Approval ID
c26c8834-961e-4c9c-9ad4-5db2d9419938
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 15, 2023
Manufacturers
FDA
ANI Pharmaceuticals, Inc.
DUNS: 145588013
Products 2
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 Code62559-241
Application NumberANDA040001
Product Classification
M
Marketing Category
C73584
G
Generic Name
Methazolamide
Product Specifications
Route of AdministrationORAL
Effective DateMay 12, 2017
FDA Product Classification
INGREDIENTS (6)
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
METHAZOLAMIDEActive
Quantity: 50 mg in 1 1
Code: W733B0S9SD
Classification: ACTIB
POVIDONE K30Inactive
Code: U725QWY32X
Classification: IACT
DIBASIC CALCIUM PHOSPHATE DIHYDRATEInactive
Code: O7TSZ97GEP
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
GLYCERYL DIBEHENATEInactive
Code: R8WTH25YS2
Classification: IACT
Methazolamide
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code62559-240
Application NumberANDA040001
Product Classification
M
Marketing Category
C73584
G
Generic Name
Methazolamide
Product Specifications
Route of AdministrationORAL
Effective DateMay 12, 2017
FDA Product Classification
INGREDIENTS (6)
METHAZOLAMIDEActive
Quantity: 25 mg in 1 1
Code: W733B0S9SD
Classification: ACTIB
POVIDONE K30Inactive
Code: U725QWY32X
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
DIBASIC CALCIUM PHOSPHATE DIHYDRATEInactive
Code: O7TSZ97GEP
Classification: IACT
GLYCERYL DIBEHENATEInactive
Code: R8WTH25YS2
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT