diazepam

Generic: diazepam

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

Drug Facts

Product Profile

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

diazepam 5 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0172-3926
Product ID 0172-3926_db225e5f-9265-4460-ab58-3305246c6258
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071321
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 1986-12-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01723926
Hyphenated Format 0172-3926

Supplemental Identifiers

RxCUI
197589 197590 197591
UPC
0301723926609 0301723927606 0301723925602
UNII
Q3JTX2Q7TU
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 diazepam (source: ndc)
Generic Name diazepam (source: ndc)
Application Number ANDA071321 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0172-3926-60)
  • 500 TABLET in 1 BOTTLE (0172-3926-70)
  • 1000 TABLET in 1 BOTTLE (0172-3926-80)
source: ndc

Packages (3)

0172-3926-60 100 TABLET in 1 BOTTLE (0172-3926-60) 0172-3926-70 500 TABLET in 1 BOTTLE (0172-3926-70) 0172-3926-80 1000 TABLET in 1 BOTTLE (0172-3926-80)

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": "db225e5f-9265-4460-ab58-3305246c6258", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0301723926609", "0301723927606", "0301723925602"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197589", "197590", "197591"], "spl_set_id": ["48aa32cb-047a-414a-822e-82a5f26d8817"], "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 (0172-3926-60)", "package_ndc": "0172-3926-60", "marketing_start_date": "19861210"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0172-3926-70)", "package_ndc": "0172-3926-70", "marketing_start_date": "19861210"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (0172-3926-80)", "package_ndc": "0172-3926-80", "marketing_start_date": "19861210"}], "brand_name": "Diazepam", "product_id": "0172-3926_db225e5f-9265-4460-ab58-3305246c6258", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "0172-3926", "dea_schedule": "CIV", "generic_name": "Diazepam", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazepam", "active_ingredients": [{"name": "DIAZEPAM", "strength": "5 mg/1"}], "application_number": "ANDA071321", "marketing_category": "ANDA", "marketing_start_date": "19861210", "listing_expiration_date": "20261231"}