triazolam

Generic: triazolam

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name triazolam
Generic Name triazolam
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

triazolam .25 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-349
Product ID 72789-349_40bb635a-95e9-a7d3-e063-6294a90a6ed5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214219
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2020-10-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789349
Hyphenated Format 72789-349

Supplemental Identifiers

RxCUI
198318
UPC
0372789349305
UNII
1HM943223R
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 triazolam (source: ndc)
Generic Name triazolam (source: ndc)
Application Number ANDA214219 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (72789-349-30)
source: ndc

Packages (1)

Ingredients (1)

triazolam (.25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40bb635a-95e9-a7d3-e063-6294a90a6ed5", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0372789349305"], "unii": ["1HM943223R"], "rxcui": ["198318"], "spl_set_id": ["f8ca4773-e201-4cb9-8869-5ee07ba1d0bf"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-349-30)", "package_ndc": "72789-349-30", "marketing_start_date": "20230817"}], "brand_name": "Triazolam", "product_id": "72789-349_40bb635a-95e9-a7d3-e063-6294a90a6ed5", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72789-349", "dea_schedule": "CIV", "generic_name": "Triazolam", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Triazolam", "active_ingredients": [{"name": "TRIAZOLAM", "strength": ".25 mg/1"}], "application_number": "ANDA214219", "marketing_category": "ANDA", "marketing_start_date": "20201020", "listing_expiration_date": "20261231"}