clonazepam
Generic: clonazepam
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
clonazepam
Generic Name
clonazepam
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
clonazepam 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4074
Product ID
70518-4074_4c99b19a-49cc-877f-e063-6294a90afe01
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075150
DEA Schedule
civ
Listing Expiration
2027-12-31
Marketing Start
2024-05-10
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184074
Hyphenated Format
70518-4074
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
ANDA075150 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 30 TABLET in 1 BLISTER PACK (70518-4074-0)
- 30 TABLET in 1 BLISTER PACK (70518-4074-3)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4c99b19a-49cc-877f-e063-6294a90afe01", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["5PE9FDE8GB"], "rxcui": ["197528"], "spl_set_id": ["2606ecf9-3d71-4c1c-bfda-d7d98ffc6011"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4074-0)", "package_ndc": "70518-4074-0", "marketing_start_date": "20240510"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4074-3)", "package_ndc": "70518-4074-3", "marketing_start_date": "20241118"}], "brand_name": "Clonazepam", "product_id": "70518-4074_4c99b19a-49cc-877f-e063-6294a90afe01", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "70518-4074", "dea_schedule": "CIV", "generic_name": "Clonazepam", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonazepam", "active_ingredients": [{"name": "CLONAZEPAM", "strength": "1 mg/1"}], "application_number": "ANDA075150", "marketing_category": "ANDA", "marketing_start_date": "20240510", "listing_expiration_date": "20271231"}