clonazepam
Generic: clonazepam
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
clonazepam
Generic Name
clonazepam
Labeler
a-s medication solutions
Dosage Form
TABLET, ORALLY DISINTEGRATING
Routes
Active Ingredients
clonazepam .5 mg/1
Manufacturer
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)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500907555
Hyphenated Format
50090-7555
Supplemental Identifiers
RxCUI
UNII
NUI
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
source: ndc
Resolved Composition
Strengths
- .5 mg/1
Packaging
- 60 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (50090-7555-0)
Packages (1)
Ingredients (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"}