clonazepam

Generic: clonazepam

Labeler: advanced rx pharmacy of tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonazepam
Generic Name clonazepam
Labeler advanced rx pharmacy of tennessee, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clonazepam 1 mg/1

Manufacturer
Advanced Rx Pharmacy of Tennessee, LLC

Identifiers & Regulatory

Product NDC 80425-0135
Product ID 80425-0135_2a99b834-0c98-6f97-e063-6394a90a8407
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077147
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2011-06-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 804250135
Hyphenated Format 80425-0135

Supplemental Identifiers

RxCUI
197528
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 ANDA077147 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (80425-0135-1)
  • 60 TABLET in 1 BOTTLE (80425-0135-2)
  • 90 TABLET in 1 BOTTLE (80425-0135-3)
source: ndc

Packages (3)

Ingredients (1)

clonazepam (1 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a99b834-0c98-6f97-e063-6394a90a8407", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["5PE9FDE8GB"], "rxcui": ["197528"], "spl_set_id": ["be383e56-d71f-7699-e053-2995a90a50c1"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80425-0135-1)", "package_ndc": "80425-0135-1", "marketing_start_date": "20110603"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0135-2)", "package_ndc": "80425-0135-2", "marketing_start_date": "20110603"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (80425-0135-3)", "package_ndc": "80425-0135-3", "marketing_start_date": "20110603"}], "brand_name": "Clonazepam", "product_id": "80425-0135_2a99b834-0c98-6f97-e063-6394a90a8407", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "80425-0135", "dea_schedule": "CIV", "generic_name": "Clonazepam", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonazepam", "active_ingredients": [{"name": "CLONAZEPAM", "strength": "1 mg/1"}], "application_number": "ANDA077147", "marketing_category": "ANDA", "marketing_start_date": "20110603", "listing_expiration_date": "20261231"}