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, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

alprazolam 1 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-445
Product ID 63187-445_7522bce9-9d0b-4cf7-a57b-86301bbef471
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090871
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2011-06-07

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63187445
Hyphenated Format 63187-445

Supplemental Identifiers

RxCUI
433800
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 ANDA090871 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-445-30)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-445-60)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-445-90)
source: ndc

Packages (3)

Ingredients (1)

alprazolam (1 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7522bce9-9d0b-4cf7-a57b-86301bbef471", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["433800"], "spl_set_id": ["34631dbf-f817-484d-8bcf-f8efa07178d7"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-445-30)", "package_ndc": "63187-445-30", "marketing_start_date": "20181201"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-445-60)", "package_ndc": "63187-445-60", "marketing_start_date": "20181201"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-445-90)", "package_ndc": "63187-445-90", "marketing_start_date": "20181201"}], "brand_name": "Alprazolam", "product_id": "63187-445_7522bce9-9d0b-4cf7-a57b-86301bbef471", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "63187-445", "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": "1 mg/1"}], "application_number": "ANDA090871", "marketing_category": "ANDA", "marketing_start_date": "20110607", "listing_expiration_date": "20261231"}