triazolam

Generic: triazolam

Labeler: zydus pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

triazolam .25 mg/1

Manufacturer
Zydus Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 70710-1289
Product ID 70710-1289_4c2fb12f-623b-4dc9-a9e0-7fac953f5cf0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213003
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2022-12-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707101289
Hyphenated Format 70710-1289

Supplemental Identifiers

RxCUI
198317 198318
UPC
0370710128913 0370710152116
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 ANDA213003 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (70710-1289-1)
  • 500 TABLET in 1 BOTTLE (70710-1289-5)
  • 10 TABLET in 1 BOTTLE (70710-1289-8)
source: ndc

Packages (3)

70710-1289-1 100 TABLET in 1 BOTTLE (70710-1289-1) 70710-1289-5 500 TABLET in 1 BOTTLE (70710-1289-5) 70710-1289-8 10 TABLET in 1 BOTTLE (70710-1289-8)

Ingredients (1)

triazolam (.25 mg/1)

Linked Drug Pages (1)

Triazolam ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4c2fb12f-623b-4dc9-a9e0-7fac953f5cf0", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0370710128913", "0370710152116"], "unii": ["1HM943223R"], "rxcui": ["198317", "198318"], "spl_set_id": ["8d414eb8-eec9-486f-90fc-00eed0cf7daf"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70710-1289-1)", "package_ndc": "70710-1289-1", "marketing_start_date": "20221230"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70710-1289-5)", "package_ndc": "70710-1289-5", "marketing_start_date": "20221230"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (70710-1289-8)", "package_ndc": "70710-1289-8", "marketing_start_date": "20221230"}], "brand_name": "Triazolam", "product_id": "70710-1289_4c2fb12f-623b-4dc9-a9e0-7fac953f5cf0", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "70710-1289", "dea_schedule": "CIV", "generic_name": "Triazolam", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Triazolam", "active_ingredients": [{"name": "TRIAZOLAM", "strength": ".25 mg/1"}], "application_number": "ANDA213003", "marketing_category": "ANDA", "marketing_start_date": "20221230", "listing_expiration_date": "20261231"}