clonazepam

Generic: clonazepam

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonazepam
Generic Name clonazepam
Labeler northstar rx llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clonazepam 1 mg/1

Manufacturer
Northstar Rx LLC

Identifiers & Regulatory

Product NDC 72603-308
Product ID 72603-308_4764ed40-0c42-835c-e063-6394a90a9b68
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075468
DEA Schedule civ
Listing Expiration 2027-12-31
Marketing Start 2000-10-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72603308
Hyphenated Format 72603-308

Supplemental Identifiers

RxCUI
197527 197528 197529
UPC
0372603307023 0372603307016 0372603309027 0372603309010 0372603308020 0372603308037
UNII
5PE9FDE8GB
NUI
N0000175694 M0002356

Packaging Origin

Original Packager
true

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 ANDA075468 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72603-308-01)
  • 500 TABLET in 1 BOTTLE (72603-308-02)
  • 1000 TABLET in 1 BOTTLE (72603-308-03)
source: ndc

Packages (3)

Ingredients (1)

clonazepam (1 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4764ed40-0c42-835c-e063-6394a90a9b68", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0372603307023", "0372603307016", "0372603309027", "0372603309010", "0372603308020", "0372603308037"], "unii": ["5PE9FDE8GB"], "rxcui": ["197527", "197528", "197529"], "spl_set_id": ["017534e6-49ff-45f3-b88f-2f34cf0cf8fd"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72603-308-01)", "package_ndc": "72603-308-01", "marketing_start_date": "20241101"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72603-308-02)", "package_ndc": "72603-308-02", "marketing_start_date": "20241101"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (72603-308-03)", "package_ndc": "72603-308-03", "marketing_start_date": "20241101"}], "brand_name": "Clonazepam", "product_id": "72603-308_4764ed40-0c42-835c-e063-6394a90a9b68", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72603-308", "dea_schedule": "CIV", "generic_name": "Clonazepam", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonazepam", "active_ingredients": [{"name": "CLONAZEPAM", "strength": "1 mg/1"}], "application_number": "ANDA075468", "marketing_category": "ANDA", "marketing_start_date": "20001006", "listing_expiration_date": "20271231"}