Methazolamide
Methazolamide Tablets USP Rx only
Approved
Approval ID
1698aa2d-a962-4bcc-8646-4fff532b645b
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 9, 2024
Manufacturers
FDA
Bryant Ranch Prepack
DUNS: 171714327
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 Code63629-1987
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: 50 mg in 1 1
Code: W733B0S9SD
Classification: ACTIB
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
GLYCERYL DIBEHENATEInactive
Code: R8WTH25YS2
Classification: IACT
DIBASIC CALCIUM PHOSPHATE DIHYDRATEInactive
Code: O7TSZ97GEP
Classification: IACT
POVIDONE K30Inactive
Code: U725QWY32X
Classification: IACT