diazepam

Generic: diazepam

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diazepam
Generic Name diazepam
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

diazepam 2 mg/1

Manufacturer
Direct_rx

Identifiers & Regulatory

Product NDC 72189-570
Product ID 72189-570_2047f721-6a06-c391-e063-6394a90a4ed7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070325
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2024-08-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189570
Hyphenated Format 72189-570

Supplemental Identifiers

RxCUI
197590
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
  • 2 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (72189-570-30)
source: ndc

Packages (1)

72189-570-30 30 TABLET in 1 BOTTLE, PLASTIC (72189-570-30)

Ingredients (1)

diazepam (2 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": "2047f721-6a06-c391-e063-6394a90a4ed7", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197590"], "spl_set_id": ["2047f721-6a05-c391-e063-6394a90a4ed7"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Direct_rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72189-570-30)", "package_ndc": "72189-570-30", "marketing_start_date": "20240822"}], "brand_name": "Diazepam", "product_id": "72189-570_2047f721-6a06-c391-e063-6394a90a4ed7", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72189-570", "dea_schedule": "CIV", "generic_name": "Diazepam", "labeler_name": "Direct_rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazepam", "active_ingredients": [{"name": "DIAZEPAM", "strength": "2 mg/1"}], "application_number": "ANDA070325", "marketing_category": "ANDA", "marketing_start_date": "20240822", "listing_expiration_date": "20261231"}