triazolam

Generic: triazolam

Labeler: ingenus pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name triazolam
Generic Name triazolam
Labeler ingenus pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

triazolam .25 mg/1

Manufacturer
Ingenus Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 50742-646
Product ID 50742-646_22a3bdbc-8edf-45a5-ad5c-4a0c3f73f255
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 50742646
Hyphenated Format 50742-646

Supplemental Identifiers

RxCUI
198317 198318
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 ANDA214219 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (50742-646-01)
  • 500 TABLET in 1 BOTTLE, PLASTIC (50742-646-05)
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": "22a3bdbc-8edf-45a5-ad5c-4a0c3f73f255", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["1HM943223R"], "rxcui": ["198317", "198318"], "spl_set_id": ["a0c99f0b-4122-4611-9b53-80fadfceacb6"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (50742-646-01)", "package_ndc": "50742-646-01", "marketing_start_date": "20201020"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (50742-646-05)", "package_ndc": "50742-646-05", "marketing_start_date": "20201020"}], "brand_name": "Triazolam", "product_id": "50742-646_22a3bdbc-8edf-45a5-ad5c-4a0c3f73f255", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "50742-646", "dea_schedule": "CIV", "generic_name": "Triazolam", "labeler_name": "Ingenus Pharmaceuticals, LLC", "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"}