clonazepam

Generic: clonazepam

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

clonazepam .5 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-307
Product ID 72789-307_401fa400-c30b-f23e-e063-6394a90a0137
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077856
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2018-02-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789307
Hyphenated Format 72789-307

Supplemental Identifiers

RxCUI
197527
UPC
0372789307305
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 ANDA077856 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (72789-307-30)
source: ndc

Packages (1)

Ingredients (1)

clonazepam (.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "401fa400-c30b-f23e-e063-6394a90a0137", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0372789307305"], "unii": ["5PE9FDE8GB"], "rxcui": ["197527"], "spl_set_id": ["08d0a109-3307-47b5-8ff2-c0ad83e66f08"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-307-30)", "package_ndc": "72789-307-30", "marketing_start_date": "20220306"}], "brand_name": "Clonazepam", "product_id": "72789-307_401fa400-c30b-f23e-e063-6394a90a0137", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72789-307", "dea_schedule": "CIV", "generic_name": "clonazepam", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonazepam", "active_ingredients": [{"name": "CLONAZEPAM", "strength": ".5 mg/1"}], "application_number": "ANDA077856", "marketing_category": "ANDA", "marketing_start_date": "20180215", "listing_expiration_date": "20261231"}