clonazepam
Generic: clonazepam
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
clonazepam
Generic Name
clonazepam
Labeler
major pharmaceuticals
Dosage Form
TABLET
Routes
Active Ingredients
clonazepam 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0904-7728
Product ID
0904-7728_8a2394b5-5506-4279-a197-8955379df72d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077856
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2022-08-23
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09047728
Hyphenated Format
0904-7728
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
ANDA077856 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 100 BLISTER PACK in 1 CARTON (0904-7728-61) / 1 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8a2394b5-5506-4279-a197-8955379df72d", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["5PE9FDE8GB"], "rxcui": ["197527", "197528"], "spl_set_id": ["34366dd2-432c-4fa9-8fab-832cca781b84"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7728-61) / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7728-61", "marketing_start_date": "20220823"}], "brand_name": "Clonazepam", "product_id": "0904-7728_8a2394b5-5506-4279-a197-8955379df72d", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "0904-7728", "dea_schedule": "CIV", "generic_name": "clonazepam", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonazepam", "active_ingredients": [{"name": "CLONAZEPAM", "strength": "1 mg/1"}], "application_number": "ANDA077856", "marketing_category": "ANDA", "marketing_start_date": "20220823", "listing_expiration_date": "20261231"}