clonazepam

Generic: clonazepam

Labeler: preferred pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonazepam
Generic Name clonazepam
Labeler preferred pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clonazepam 1 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-7738
Product ID 68788-7738_93676957-0121-4562-ad3c-28e3d267c13b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077147
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2020-07-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887738
Hyphenated Format 68788-7738

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
  • 20 TABLET in 1 BOTTLE, PLASTIC (68788-7738-2)
  • 30 TABLET in 1 BOTTLE, PLASTIC (68788-7738-3)
  • 60 TABLET in 1 BOTTLE, PLASTIC (68788-7738-6)
  • 28 TABLET in 1 BOTTLE, PLASTIC (68788-7738-8)
  • 90 TABLET in 1 BOTTLE, PLASTIC (68788-7738-9)
source: ndc

Packages (5)

68788-7738-2 20 TABLET in 1 BOTTLE, PLASTIC (68788-7738-2) 68788-7738-3 30 TABLET in 1 BOTTLE, PLASTIC (68788-7738-3) 68788-7738-6 60 TABLET in 1 BOTTLE, PLASTIC (68788-7738-6) 68788-7738-8 28 TABLET in 1 BOTTLE, PLASTIC (68788-7738-8) 68788-7738-9 90 TABLET in 1 BOTTLE, PLASTIC (68788-7738-9)

Ingredients (1)

clonazepam (1 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": "93676957-0121-4562-ad3c-28e3d267c13b", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["5PE9FDE8GB"], "rxcui": ["197528"], "spl_set_id": ["2dc15db1-9dff-4be9-8e73-35a01c5aea32"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (68788-7738-2)", "package_ndc": "68788-7738-2", "marketing_start_date": "20200701"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (68788-7738-3)", "package_ndc": "68788-7738-3", "marketing_start_date": "20200701"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (68788-7738-6)", "package_ndc": "68788-7738-6", "marketing_start_date": "20200701"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE, PLASTIC (68788-7738-8)", "package_ndc": "68788-7738-8", "marketing_start_date": "20200701"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (68788-7738-9)", "package_ndc": "68788-7738-9", "marketing_start_date": "20200701"}], "brand_name": "Clonazepam", "product_id": "68788-7738_93676957-0121-4562-ad3c-28e3d267c13b", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "68788-7738", "dea_schedule": "CIV", "generic_name": "clonazepam", "labeler_name": "Preferred Pharmaceuticals, Inc.", "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": "20200701", "listing_expiration_date": "20261231"}