valium

Generic: diazepam

Labeler: roche laboratories inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name valium
Generic Name diazepam
Labeler roche laboratories inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

diazepam 2 mg/1

Manufacturer
Roche Laboratories Inc.

Identifiers & Regulatory

Product NDC 0140-0004
Product ID 0140-0004_ea505cdb-6d89-4b8c-8007-ec5a5fe920ce
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA013263
DEA Schedule civ
Marketing Start 1963-11-15
Marketing End 2027-08-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01400004
Hyphenated Format 0140-0004

Supplemental Identifiers

RxCUI
104699 104700 197590 197591
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 valium (source: ndc)
Generic Name diazepam (source: ndc)
Application Number NDA013263 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (0140-0004-01) / 100 TABLET in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

0140-0004-01 1 BOTTLE, PLASTIC in 1 CARTON (0140-0004-01) / 100 TABLET in 1 BOTTLE, PLASTIC

Ingredients (1)

diazepam (2 mg/1)

Linked Drug Pages (1)

Valium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ea505cdb-6d89-4b8c-8007-ec5a5fe920ce", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["104699", "104700", "197590", "197591"], "spl_set_id": ["554baee5-b171-4452-a50a-41a0946f956c"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Roche Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (0140-0004-01)  / 100 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "0140-0004-01", "marketing_end_date": "20270810", "marketing_start_date": "19631115"}], "brand_name": "Valium", "product_id": "0140-0004_ea505cdb-6d89-4b8c-8007-ec5a5fe920ce", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "0140-0004", "dea_schedule": "CIV", "generic_name": "diazepam", "labeler_name": "Roche Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valium", "active_ingredients": [{"name": "DIAZEPAM", "strength": "2 mg/1"}], "application_number": "NDA013263", "marketing_category": "NDA", "marketing_end_date": "20270810", "marketing_start_date": "19631115"}