diazepam

Generic: diazepam

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diazepam
Generic Name diazepam
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

diazepam 10 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1726
Product ID 50090-1726_8b32cbef-f70b-4b28-b267-9768b7a40197
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071322
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 500901726
Hyphenated Format 50090-1726

Supplemental Identifiers

RxCUI
197589 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 ANDA071322 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (50090-1726-0)
  • 30 TABLET in 1 BOTTLE (50090-1726-2)
  • 60 TABLET in 1 BOTTLE (50090-1726-3)
source: ndc

Packages (3)

50090-1726-0 100 TABLET in 1 BOTTLE (50090-1726-0) 50090-1726-2 30 TABLET in 1 BOTTLE (50090-1726-2) 50090-1726-3 60 TABLET in 1 BOTTLE (50090-1726-3)

Ingredients (1)

diazepam (10 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": "8b32cbef-f70b-4b28-b267-9768b7a40197", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197589", "197591"], "spl_set_id": ["b47dc708-e83b-4224-bdb5-c9b7abd35cfb"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-1726-0)", "package_ndc": "50090-1726-0", "marketing_start_date": "20150305"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-1726-2)", "package_ndc": "50090-1726-2", "marketing_start_date": "20150305"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-1726-3)", "package_ndc": "50090-1726-3", "marketing_start_date": "20150305"}], "brand_name": "Diazepam", "product_id": "50090-1726_8b32cbef-f70b-4b28-b267-9768b7a40197", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "50090-1726", "dea_schedule": "CIV", "generic_name": "Diazepam", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazepam", "active_ingredients": [{"name": "DIAZEPAM", "strength": "10 mg/1"}], "application_number": "ANDA071322", "marketing_category": "ANDA", "marketing_start_date": "19861210", "listing_expiration_date": "20261231"}