AcetaZOLAMIDE
AcetaZOLAMIDE TABLETS USP
Approved
Approval ID
6972d9c1-36ec-4246-bf7b-13206d5952c3
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 5, 2011
Manufacturers
FDA
RedPharm Drug Inc.
DUNS: 008039641
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Acetazolamide
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code67296-0801
Application NumberANDA084840
Product Classification
M
Marketing Category
C73584
G
Generic Name
Acetazolamide
Product Specifications
Route of AdministrationORAL
Effective DateAugust 5, 2011
FDA Product Classification
INGREDIENTS (5)
ACETAZOLAMIDEActive
Quantity: 250 1 in 1 1
Code: O3FX965V0I
Classification: ACTIB
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
CALCIUM STEARATEInactive
Code: 776XM7047L
Classification: IACT