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
NDC Product Code50090-2823
Application NumberANDA074869
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateNovember 21, 2017
Generic NameClonazepam
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