xanax

Generic: alprazolam

Labeler: viatris specialty llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name xanax
Generic Name alprazolam
Labeler viatris specialty llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alprazolam 1 mg/1

Manufacturer
Viatris Specialty LLC

Identifiers & Regulatory

Product NDC 58151-454
Product ID 58151-454_27062ff4-9ce3-4d8a-aeae-f4468efb623a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018276
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2025-10-02

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58151454
Hyphenated Format 58151-454

Supplemental Identifiers

RxCUI
141927 141928 197321 197322 214003 214004 308047 308048
UPC
0358151455010 0358151454013 0358151452019 0358151453016
UNII
YU55MQ3IZY
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 xanax (source: ndc)
Generic Name alprazolam (source: ndc)
Application Number NDA018276 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (58151-454-01)
  • 500 TABLET in 1 BOTTLE (58151-454-05)
source: ndc

Packages (2)

58151-454-01 100 TABLET in 1 BOTTLE (58151-454-01) 58151-454-05 500 TABLET in 1 BOTTLE (58151-454-05)

Ingredients (1)

alprazolam (1 mg/1)

Linked Drug Pages (1)

Xanax ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "27062ff4-9ce3-4d8a-aeae-f4468efb623a", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0358151455010", "0358151454013", "0358151452019", "0358151453016"], "unii": ["YU55MQ3IZY"], "rxcui": ["141927", "141928", "197321", "197322", "214003", "214004", "308047", "308048"], "spl_set_id": ["bb5cf72e-3a41-41a8-9a38-80f974eca33f"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Viatris Specialty LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (58151-454-01)", "package_ndc": "58151-454-01", "marketing_start_date": "20251002"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (58151-454-05)", "package_ndc": "58151-454-05", "marketing_start_date": "20251211"}], "brand_name": "Xanax", "product_id": "58151-454_27062ff4-9ce3-4d8a-aeae-f4468efb623a", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "58151-454", "dea_schedule": "CIV", "generic_name": "alprazolam", "labeler_name": "Viatris Specialty LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Xanax", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": "1 mg/1"}], "application_number": "NDA018276", "marketing_category": "NDA", "marketing_start_date": "20251002", "listing_expiration_date": "20261231"}