clonazepam
Generic: clonazepam
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
clonazepam
Generic Name
clonazepam
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
clonazepam 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43063-794
Product ID
43063-794_415b681a-3c14-e26d-e063-6394a90a2fcb
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077147
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2011-06-03
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43063794
Hyphenated Format
43063-794
Supplemental Identifiers
RxCUI
UPC
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
ANDA077147 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (43063-794-30)
- 60 TABLET in 1 BOTTLE, PLASTIC (43063-794-60)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "415b681a-3c14-e26d-e063-6394a90a2fcb", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0343063794302"], "unii": ["5PE9FDE8GB"], "rxcui": ["197528"], "spl_set_id": ["9ee4e019-6a99-4aac-84b0-9aae597815a7"], "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 (43063-794-30)", "package_ndc": "43063-794-30", "marketing_start_date": "20171010"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-794-60)", "package_ndc": "43063-794-60", "marketing_start_date": "20171010"}], "brand_name": "Clonazepam", "product_id": "43063-794_415b681a-3c14-e26d-e063-6394a90a2fcb", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "43063-794", "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": "1 mg/1"}], "application_number": "ANDA077147", "marketing_category": "ANDA", "marketing_start_date": "20110603", "listing_expiration_date": "20261231"}