xanax

Generic: alprazolam

Labeler: pharmacia & upjohn company llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name xanax
Generic Name alprazolam
Labeler pharmacia & upjohn company llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alprazolam .25 mg/1

Manufacturer
PHARMACIA & UPJOHN COMPANY LLC

Identifiers & Regulatory

Product NDC 0009-0029
Product ID 0009-0029_f5323eac-81d0-4096-ac15-2f25220c5c28
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018276
DEA Schedule civ
Marketing Start 1981-10-16
Marketing End 2026-10-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00090029
Hyphenated Format 0009-0029

Supplemental Identifiers

RxCUI
141927 141928 197321 197322 214003 214004 308047 308048
UPC
0300090094010 0300090090012 0300090029012 0300090055011
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
  • .25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0009-0029-01)
  • 500 TABLET in 1 BOTTLE (0009-0029-02)
source: ndc

Packages (2)

0009-0029-01 100 TABLET in 1 BOTTLE (0009-0029-01) 0009-0029-02 500 TABLET in 1 BOTTLE (0009-0029-02)

Ingredients (1)

alprazolam (.25 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": "f5323eac-81d0-4096-ac15-2f25220c5c28", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0300090094010", "0300090090012", "0300090029012", "0300090055011"], "unii": ["YU55MQ3IZY"], "rxcui": ["141927", "141928", "197321", "197322", "214003", "214004", "308047", "308048"], "spl_set_id": ["388e249d-b9b6-44c3-9f8f-880eced0239f"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["PHARMACIA & UPJOHN COMPANY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0009-0029-01)", "package_ndc": "0009-0029-01", "marketing_end_date": "20261031", "marketing_start_date": "19811016"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0009-0029-02)", "package_ndc": "0009-0029-02", "marketing_end_date": "20261031", "marketing_start_date": "19811016"}], "brand_name": "Xanax", "product_id": "0009-0029_f5323eac-81d0-4096-ac15-2f25220c5c28", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "0009-0029", "dea_schedule": "CIV", "generic_name": "alprazolam", "labeler_name": "PHARMACIA & UPJOHN COMPANY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Xanax", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": ".25 mg/1"}], "application_number": "NDA018276", "marketing_category": "NDA", "marketing_end_date": "20261031", "marketing_start_date": "19811016"}