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 2 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-0195
Product ID 50090-0195_be411eaf-14d8-40ad-982e-8602f293e00d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071307
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 500900195
Hyphenated Format 50090-0195

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 ANDA071307 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 2 TABLET in 1 BOTTLE (50090-0195-6)
source: ndc

Packages (1)

50090-0195-6 2 TABLET in 1 BOTTLE (50090-0195-6)

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": "be411eaf-14d8-40ad-982e-8602f293e00d", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197590"], "spl_set_id": ["ec433be5-d84d-425f-9edf-71263f885eec"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET in 1 BOTTLE (50090-0195-6)", "package_ndc": "50090-0195-6", "marketing_start_date": "20141128"}], "brand_name": "Diazepam", "product_id": "50090-0195_be411eaf-14d8-40ad-982e-8602f293e00d", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "50090-0195", "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": "2 mg/1"}], "application_number": "ANDA071307", "marketing_category": "ANDA", "marketing_start_date": "19861210", "listing_expiration_date": "20261231"}