alprazolam

Generic: alprazolam

Labeler: advanced rx of tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alprazolam
Generic Name alprazolam
Labeler advanced rx of tennessee, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alprazolam 1 mg/1

Manufacturer
Advanced Rx of Tennessee, LLC

Identifiers & Regulatory

Product NDC 80425-0110
Product ID 80425-0110_2a99a7f4-89df-19db-e063-6294a90a90da
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074342
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 1993-10-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 804250110
Hyphenated Format 80425-0110

Supplemental Identifiers

RxCUI
197321
UNII
YU55MQ3IZY
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 alprazolam (source: ndc)
Generic Name alprazolam (source: ndc)
Application Number ANDA074342 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (80425-0110-2)
source: ndc

Packages (1)

80425-0110-2 60 TABLET in 1 BOTTLE (80425-0110-2)

Ingredients (1)

alprazolam (1 mg/1)

Linked Drug Pages (1)

Alprazolam ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a99a7f4-89df-19db-e063-6294a90a90da", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321"], "spl_set_id": ["b4cd647f-1ba3-334e-e053-2995a90af352"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0110-2)", "package_ndc": "80425-0110-2", "marketing_start_date": "19931001"}], "brand_name": "Alprazolam", "product_id": "80425-0110_2a99a7f4-89df-19db-e063-6294a90a90da", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "80425-0110", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": "1 mg/1"}], "application_number": "ANDA074342", "marketing_category": "ANDA", "marketing_start_date": "19931001", "listing_expiration_date": "20261231"}