alprazolam

Generic: alprazolam

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alprazolam
Generic Name alprazolam
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alprazolam 2 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-444
Product ID 63187-444_525278ca-7947-41ac-92cf-b5a4e90dc56c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074909
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 1998-03-25

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63187444
Hyphenated Format 63187-444

Supplemental Identifiers

RxCUI
197321 197322 308048
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 ANDA074909 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (63187-444-30)
  • 60 TABLET in 1 BOTTLE (63187-444-60)
  • 90 TABLET in 1 BOTTLE (63187-444-90)
source: ndc

Packages (3)

Ingredients (1)

alprazolam (2 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "525278ca-7947-41ac-92cf-b5a4e90dc56c", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321", "197322", "308048"], "spl_set_id": ["717ce509-f92e-4ec1-a3c6-aeae54d56f4d"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-444-30)", "package_ndc": "63187-444-30", "marketing_start_date": "20140303"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-444-60)", "package_ndc": "63187-444-60", "marketing_start_date": "20140303"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63187-444-90)", "package_ndc": "63187-444-90", "marketing_start_date": "20140303"}], "brand_name": "Alprazolam", "product_id": "63187-444_525278ca-7947-41ac-92cf-b5a4e90dc56c", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "63187-444", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": "2 mg/1"}], "application_number": "ANDA074909", "marketing_category": "ANDA", "marketing_start_date": "19980325", "listing_expiration_date": "20261231"}