alprazolam

Generic: alprazolam

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alprazolam
Generic Name alprazolam
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alprazolam 2 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 55289-523
Product ID 55289-523_2abee2c1-1fa5-af2e-e063-6294a90a6afb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074909
DEA Schedule civ
Marketing Start 1998-03-25
Marketing End 2027-03-19

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55289523
Hyphenated Format 55289-523

Supplemental Identifiers

RxCUI
197322
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
  • 100 TABLET in 1 BOTTLE, PLASTIC (55289-523-01)
  • 30 TABLET in 1 BOTTLE, PLASTIC (55289-523-30)
  • 40 TABLET in 1 BOTTLE, PLASTIC (55289-523-40)
  • 60 TABLET in 1 BOTTLE, PLASTIC (55289-523-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (55289-523-90)
source: ndc

Packages (5)

55289-523-01 100 TABLET in 1 BOTTLE, PLASTIC (55289-523-01) 55289-523-30 30 TABLET in 1 BOTTLE, PLASTIC (55289-523-30) 55289-523-40 40 TABLET in 1 BOTTLE, PLASTIC (55289-523-40) 55289-523-60 60 TABLET in 1 BOTTLE, PLASTIC (55289-523-60) 55289-523-90 90 TABLET in 1 BOTTLE, PLASTIC (55289-523-90)

Ingredients (1)

alprazolam (2 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": "2abee2c1-1fa5-af2e-e063-6294a90a6afb", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["197322"], "spl_set_id": ["7538d0d0-346e-4c3e-8f7a-c1cac8ec8ed3"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (55289-523-01)", "package_ndc": "55289-523-01", "marketing_end_date": "20270319", "marketing_start_date": "20160304"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (55289-523-30)", "package_ndc": "55289-523-30", "marketing_end_date": "20270319", "marketing_start_date": "20160304"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE, PLASTIC (55289-523-40)", "package_ndc": "55289-523-40", "marketing_end_date": "20270319", "marketing_start_date": "20160304"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (55289-523-60)", "package_ndc": "55289-523-60", "marketing_end_date": "20270319", "marketing_start_date": "20160304"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (55289-523-90)", "package_ndc": "55289-523-90", "marketing_end_date": "20270319", "marketing_start_date": "20160304"}], "brand_name": "Alprazolam", "product_id": "55289-523_2abee2c1-1fa5-af2e-e063-6294a90a6afb", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "55289-523", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": "2 mg/1"}], "application_number": "ANDA074909", "marketing_category": "ANDA", "marketing_end_date": "20270319", "marketing_start_date": "19980325"}