FDA.reportPublic FDA data

Clonazepam

Product NDC
35356-722
11-digit product format
353560722
Labeler code
35356
Product ID
35356-722_8e30d57b-61ba-490c-aab6-08bd01a9b66d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Clonazepam
Dosage form
TABLET
Route
ORAL
Labeler
Quality Care Products, LLC
Application
ANDA074569
Marketing category
ANDA
Marketing start
1996-09-17
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
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
35356-722-002025-01-16C16284748780-1ba0f9c33-33d8-a910-e053-dadaa90a0b85ec134b69-3d24-44d3-b890-7ea641f5e502
35356-722-302025-01-16C16284748780-1ba0f9c33-33d8-a910-e053-dadaa90a0b85ec134b69-3d24-44d3-b890-7ea641f5e502
35356-722-602025-01-16C16284748780-1ba0f9c33-33d8-a910-e053-dadaa90a0b85ec134b69-3d24-44d3-b890-7ea641f5e502
35356-722-902025-01-16C16284748780-1ba0f9c33-33d8-a910-e053-dadaa90a0b85ec134b69-3d24-44d3-b890-7ea641f5e502
35356-722-002021-01-29C16284748780-1ba0f9c33-33d8-a910-e053-dadaa90a0b85ec134b69-3d24-44d3-b890-7ea641f5e502
35356-722-302021-01-29C16284748780-1ba0f9c33-33d8-a910-e053-dadaa90a0b85ec134b69-3d24-44d3-b890-7ea641f5e502
35356-722-602021-01-29C16284748780-1ba0f9c33-33d8-a910-e053-dadaa90a0b85ec134b69-3d24-44d3-b890-7ea641f5e502
35356-722-902021-01-29C16284748780-1ba0f9c33-33d8-a910-e053-dadaa90a0b85ec134b69-3d24-44d3-b890-7ea641f5e502

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
35356-722-30EA - Each35356-72280690341-90da-4d49-b54a-b9059f21c98512013-02-13
35356-722-60EA - Each35356-72292fd2472-0495-4278-9394-eb1b3833f6a212013-02-13
35356-722-90EA - Each35356-722554bb778-e911-4cee-9656-cd1532bf089112013-02-13