diazepam

Generic: diazepam

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diazepam
Generic Name diazepam
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

diazepam 5 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8466
Product ID 68788-8466_893c2a53-0c5a-49a7-b2b5-29510111829c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070325
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2023-06-19

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888466
Hyphenated Format 68788-8466

Supplemental Identifiers

RxCUI
197591
UNII
Q3JTX2Q7TU
NUI
N0000175694 M0002356

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 diazepam (source: ndc)
Generic Name diazepam (source: ndc)
Application Number ANDA070325 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE, PLASTIC (68788-8466-2)
  • 30 TABLET in 1 BOTTLE, PLASTIC (68788-8466-3)
  • 60 TABLET in 1 BOTTLE, PLASTIC (68788-8466-6)
source: ndc

Packages (3)

68788-8466-2 20 TABLET in 1 BOTTLE, PLASTIC (68788-8466-2) 68788-8466-3 30 TABLET in 1 BOTTLE, PLASTIC (68788-8466-3) 68788-8466-6 60 TABLET in 1 BOTTLE, PLASTIC (68788-8466-6)

Ingredients (1)

diazepam (5 mg/1)

Linked Drug Pages (1)

Diazepam ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "893c2a53-0c5a-49a7-b2b5-29510111829c", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197591"], "spl_set_id": ["7646785b-dabc-482d-bf42-06177f00aca2"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (68788-8466-2)", "package_ndc": "68788-8466-2", "marketing_start_date": "20230626"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (68788-8466-3)", "package_ndc": "68788-8466-3", "marketing_start_date": "20230626"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (68788-8466-6)", "package_ndc": "68788-8466-6", "marketing_start_date": "20240409"}], "brand_name": "Diazepam", "product_id": "68788-8466_893c2a53-0c5a-49a7-b2b5-29510111829c", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "68788-8466", "dea_schedule": "CIV", "generic_name": "diazepam", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazepam", "active_ingredients": [{"name": "DIAZEPAM", "strength": "5 mg/1"}], "application_number": "ANDA070325", "marketing_category": "ANDA", "marketing_start_date": "20230619", "listing_expiration_date": "20261231"}