clonazepam

Generic: clonazepam

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonazepam
Generic Name clonazepam
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clonazepam 1 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-3212
Product ID 0093-3212_d6abe4e3-7699-4ead-95f4-739a961b23ad
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074569
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 1996-09-17

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00933212
Hyphenated Format 0093-3212

Supplemental Identifiers

RxCUI
197527 197528 197529
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 ANDA074569 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0093-3212-01)
  • 500 TABLET in 1 BOTTLE (0093-3212-05)
source: ndc

Packages (2)

0093-3212-01 100 TABLET in 1 BOTTLE (0093-3212-01) 0093-3212-05 500 TABLET in 1 BOTTLE (0093-3212-05)

Ingredients (1)

clonazepam (1 mg/1)

Linked Drug Pages (1)

Clonazepam ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d6abe4e3-7699-4ead-95f4-739a961b23ad", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["5PE9FDE8GB"], "rxcui": ["197527", "197528", "197529"], "spl_set_id": ["8069b1a0-7c06-4252-b44e-e2eef065d9b8"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0093-3212-01)", "package_ndc": "0093-3212-01", "marketing_start_date": "19960917"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0093-3212-05)", "package_ndc": "0093-3212-05", "marketing_start_date": "19980821"}], "brand_name": "Clonazepam", "product_id": "0093-3212_d6abe4e3-7699-4ead-95f4-739a961b23ad", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "0093-3212", "dea_schedule": "CIV", "generic_name": "Clonazepam", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonazepam", "active_ingredients": [{"name": "CLONAZEPAM", "strength": "1 mg/1"}], "application_number": "ANDA074569", "marketing_category": "ANDA", "marketing_start_date": "19960917", "listing_expiration_date": "20261231"}