triazolam
Generic: triazolam
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
triazolam
Generic Name
triazolam
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
triazolam .25 mg/1
Manufacturer
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)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789349
Hyphenated Format
72789-349
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
source: ndc
Resolved Composition
Strengths
- .25 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (72789-349-30)
Packages (1)
Ingredients (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"}