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 5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1913
Product ID 50090-1913_8b32cbef-f70b-4b28-b267-9768b7a40197
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 500901913
Hyphenated Format 50090-1913

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 ANDA071321 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (50090-1913-1)
  • 30 TABLET in 1 BOTTLE (50090-1913-2)
  • 10 TABLET in 1 BOTTLE (50090-1913-4)
  • 100 TABLET in 1 BOTTLE (50090-1913-5)
source: ndc

Packages (4)

Ingredients (1)

diazepam (5 mg/1)

Linked Drug Pages (1)

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": "20 TABLET in 1 BOTTLE (50090-1913-1)", "package_ndc": "50090-1913-1", "marketing_start_date": "20150702"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-1913-2)", "package_ndc": "50090-1913-2", "marketing_start_date": "20150702"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (50090-1913-4)", "package_ndc": "50090-1913-4", "marketing_start_date": "20150702"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-1913-5)", "package_ndc": "50090-1913-5", "marketing_start_date": "20150702"}], "brand_name": "Diazepam", "product_id": "50090-1913_8b32cbef-f70b-4b28-b267-9768b7a40197", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "50090-1913", "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": "5 mg/1"}], "application_number": "ANDA071321", "marketing_category": "ANDA", "marketing_start_date": "19861210", "listing_expiration_date": "20261231"}