triazolam

Generic: triazolam

Labeler: mylan pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name triazolam
Generic Name triazolam
Labeler mylan pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

triazolam .25 mg/1

Manufacturer
Mylan Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 59762-3718
Product ID 59762-3718_eb080fc0-b150-46ce-bf63-b09b47255a73
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA017892
DEA Schedule civ
Listing Expiration 2027-12-31
Marketing Start 1982-11-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 597623718
Hyphenated Format 59762-3718

Supplemental Identifiers

RxCUI
198317 198318
UPC
0359762371898 0359762371799
UNII
1HM943223R
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 triazolam (source: ndc)
Generic Name triazolam (source: ndc)
Application Number NDA017892 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .25 mg/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE (59762-3718-3)
  • 100 TABLET in 1 BOTTLE (59762-3718-9)
source: ndc

Packages (2)

Ingredients (1)

triazolam (.25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "eb080fc0-b150-46ce-bf63-b09b47255a73", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0359762371898", "0359762371799"], "unii": ["1HM943223R"], "rxcui": ["198317", "198318"], "spl_set_id": ["5add318e-11b9-42f8-b052-0d8cebb32fcf"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (59762-3718-3)", "package_ndc": "59762-3718-3", "marketing_start_date": "19821115"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (59762-3718-9)", "package_ndc": "59762-3718-9", "marketing_start_date": "20170113"}], "brand_name": "Triazolam", "product_id": "59762-3718_eb080fc0-b150-46ce-bf63-b09b47255a73", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "59762-3718", "dea_schedule": "CIV", "generic_name": "triazolam", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Triazolam", "active_ingredients": [{"name": "TRIAZOLAM", "strength": ".25 mg/1"}], "application_number": "NDA017892", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "19821115", "listing_expiration_date": "20271231"}