Clonazepam

Product NDC
70518-2467
11-digit product format
705182467
Labeler code
70518
Product ID
70518-2467_ec92e6e9-ae22-7f8a-e053-2995a90aee75
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
clonazepam
Dosage form
TABLET
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA077856
Marketing category
ANDA
Marketing start
2019-12-05
Marketing end
0000-00-00
Substance
CLONAZEPAM
Active strength
1 mg/1
Pharmacologic classes
Benzodiazepine [EPC], Benzodiazepines [CS]
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-2467CLONAZEPAM TABLET [REMEDYREPACK INC.]11Legacy NDC20250316_3c926082-d2fe-4dc0-bca4-4dd8f82f09ee.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70518-2467-07051824670030 TABLET in 1 BLISTER PACK (70518-2467-0) 30 tablet2019-12-050000-00-00NoNoCurrent
70518-2467-170518246701100 POUCH in 1 BOX (70518-2467-1) > 1 TABLET in 1 POUCH (70518-2467-2) 100 pouch2020-01-090000-00-00NoNoCurrent