clonazepam

Generic: clonazepam

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonazepam
Generic Name clonazepam
Labeler aurobindo pharma limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clonazepam .5 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-722
Product ID 59651-722_b1582eb7-af35-45d5-a52e-0e380d08527d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075150
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2023-01-17

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59651722
Hyphenated Format 59651-722

Supplemental Identifiers

RxCUI
197527 197528 197529
UNII
5PE9FDE8GB
NUI
N0000175694 M0002356

Packaging Origin

Original Packager
true

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 ANDA075150 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (59651-722-01)
  • 1000 TABLET in 1 BOTTLE (59651-722-99)
source: ndc

Packages (2)

59651-722-01 100 TABLET in 1 BOTTLE (59651-722-01) 59651-722-99 1000 TABLET in 1 BOTTLE (59651-722-99)

Ingredients (1)

clonazepam (.5 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": "b1582eb7-af35-45d5-a52e-0e380d08527d", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["5PE9FDE8GB"], "rxcui": ["197527", "197528", "197529"], "spl_set_id": ["b1582eb7-af35-45d5-a52e-0e380d08527d"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59651-722-01)", "package_ndc": "59651-722-01", "marketing_start_date": "20230117"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (59651-722-99)", "package_ndc": "59651-722-99", "marketing_start_date": "20230117"}], "brand_name": "Clonazepam", "product_id": "59651-722_b1582eb7-af35-45d5-a52e-0e380d08527d", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "59651-722", "dea_schedule": "CIV", "generic_name": "Clonazepam", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonazepam", "active_ingredients": [{"name": "CLONAZEPAM", "strength": ".5 mg/1"}], "application_number": "ANDA075150", "marketing_category": "ANDA", "marketing_start_date": "20230117", "listing_expiration_date": "20261231"}