Pyrazinamide
PYRAZINAMIDE TABLETS USP, 500 mg
Approved
Approval ID
ecee3128-a47f-4ced-a1db-4f58c5f3e9c6
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 14, 2022
Manufacturers
FDA
Akorn
DUNS: 117693100
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Pyrazinamide
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code61748-012
Application NumberANDA081319
Product Classification
M
Marketing Category
C73584
G
Generic Name
Pyrazinamide
Product Specifications
Route of AdministrationORAL
Effective DateJuly 14, 2022
FDA Product Classification
INGREDIENTS (6)
PYRAZINAMIDEActive
Quantity: 500 mg in 1 1
Code: 2KNI5N06TI
Classification: ACTIB
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
DIBASIC CALCIUM PHOSPHATE DIHYDRATEInactive
Code: O7TSZ97GEP
Classification: IACT
STEARIC ACIDInactive
Code: 4ELV7Z65AP
Classification: IACT
MICROCRYSTALLINE CELLULOSEInactive
Code: OP1R32D61U
Classification: IACT