clonazepam

Generic: clonazepam

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonazepam
Generic Name clonazepam
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clonazepam 2 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-9747
Product ID 71335-9747_f509981c-e612-40c3-b90d-73321b727f89
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075468
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2022-04-14

Pharmacologic Class

Established (EPC)
benzodiazepine [epc]
Chemical Structure
benzodiazepines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713359747
Hyphenated Format 71335-9747

Supplemental Identifiers

RxCUI
197529
UNII
5PE9FDE8GB
NUI
N0000175694 M0002356

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name clonazepam (source: ndc)
Generic Name clonazepam (source: ndc)
Application Number ANDA075468 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-9747-1)
  • 60 TABLET in 1 BOTTLE (71335-9747-2)
  • 90 TABLET in 1 BOTTLE (71335-9747-3)
  • 120 TABLET in 1 BOTTLE (71335-9747-4)
  • 10 TABLET in 1 BOTTLE (71335-9747-5)
  • 180 TABLET in 1 BOTTLE (71335-9747-6)
source: ndc

Packages (6)

71335-9747-1 30 TABLET in 1 BOTTLE (71335-9747-1) 71335-9747-2 60 TABLET in 1 BOTTLE (71335-9747-2) 71335-9747-3 90 TABLET in 1 BOTTLE (71335-9747-3) 71335-9747-4 120 TABLET in 1 BOTTLE (71335-9747-4) 71335-9747-5 10 TABLET in 1 BOTTLE (71335-9747-5) 71335-9747-6 180 TABLET in 1 BOTTLE (71335-9747-6)

Ingredients (1)

clonazepam (2 mg/1)

Linked Drug Pages (1)

Clonazepam ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f509981c-e612-40c3-b90d-73321b727f89", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["5PE9FDE8GB"], "rxcui": ["197529"], "spl_set_id": ["19475112-60da-4d53-b330-70afe28ebaf3"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-9747-1)", "package_ndc": "71335-9747-1", "marketing_start_date": "20230711"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-9747-2)", "package_ndc": "71335-9747-2", "marketing_start_date": "20230711"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-9747-3)", "package_ndc": "71335-9747-3", "marketing_start_date": "20230711"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-9747-4)", "package_ndc": "71335-9747-4", "marketing_start_date": "20230711"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-9747-5)", "package_ndc": "71335-9747-5", "marketing_start_date": "20230711"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-9747-6)", "package_ndc": "71335-9747-6", "marketing_start_date": "20230711"}], "brand_name": "Clonazepam", "product_id": "71335-9747_f509981c-e612-40c3-b90d-73321b727f89", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "71335-9747", "dea_schedule": "CIV", "generic_name": "Clonazepam", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonazepam", "active_ingredients": [{"name": "CLONAZEPAM", "strength": "2 mg/1"}], "application_number": "ANDA075468", "marketing_category": "ANDA", "marketing_start_date": "20220414", "listing_expiration_date": "20261231"}