clonazepam

Generic: clonazepam

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonazepam
Generic Name clonazepam
Labeler a-s medication solutions
Dosage Form TABLET, ORALLY DISINTEGRATING
Routes
ORAL
Active Ingredients

clonazepam .5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7555
Product ID 50090-7555_625a86a9-4b19-498f-8907-31c63cd320d4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077171
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2005-08-05

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907555
Hyphenated Format 50090-7555

Supplemental Identifiers

RxCUI
349198
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 ANDA077171 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/1
source: ndc
Packaging
  • 60 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (50090-7555-0)
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": "625a86a9-4b19-498f-8907-31c63cd320d4", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["5PE9FDE8GB"], "rxcui": ["349198"], "spl_set_id": ["08b9b8b4-d1b3-4050-8c1b-811fab8d4e1a"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (50090-7555-0)", "package_ndc": "50090-7555-0", "marketing_start_date": "20250527"}], "brand_name": "Clonazepam", "product_id": "50090-7555_625a86a9-4b19-498f-8907-31c63cd320d4", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "50090-7555", "dea_schedule": "CIV", "generic_name": "clonazepam", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonazepam", "active_ingredients": [{"name": "CLONAZEPAM", "strength": ".5 mg/1"}], "application_number": "ANDA077171", "marketing_category": "ANDA", "marketing_start_date": "20050805", "listing_expiration_date": "20261231"}