Clonazepam
CLONAZEPAM TABLETS, USP CIV
Approved
Approval ID
68bf5bfa-8357-44ed-82ff-ad80a11789c5
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 25, 2018
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.
Clonazepam
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code50090-2823
Application NumberANDA074869
Product Classification
M
Marketing Category
C73584
G
Generic Name
Clonazepam
Product Specifications
Route of AdministrationORAL
Effective DateNovember 21, 2017
FDA Product Classification
INGREDIENTS (6)
CLONAZEPAMActive
Quantity: 0.5 mg in 1 1
Code: 5PE9FDE8GB
Classification: ACTIB
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
D&C RED NO. 30Inactive
Code: 2S42T2808B
Classification: IACT
MICROCRYSTALLINE CELLULOSEInactive
Code: OP1R32D61U
Classification: IACT