alprazolam

Generic: alprazolam

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alprazolam
Generic Name alprazolam
Labeler aurobindo pharma limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alprazolam .25 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-676
Product ID 65862-676_7527aeb7-8912-404d-afb7-8c692c84422b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203346
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2015-07-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65862676
Hyphenated Format 65862-676

Supplemental Identifiers

RxCUI
197321 197322 308047 308048
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 alprazolam (source: ndc)
Generic Name alprazolam (source: ndc)
Application Number ANDA203346 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (65862-676-01)
  • 500 TABLET in 1 BOTTLE (65862-676-05)
  • 1000 TABLET in 1 BOTTLE (65862-676-99)
source: ndc

Packages (3)

65862-676-01 100 TABLET in 1 BOTTLE (65862-676-01) 65862-676-05 500 TABLET in 1 BOTTLE (65862-676-05) 65862-676-99 1000 TABLET in 1 BOTTLE (65862-676-99)

Ingredients (1)

alprazolam (.25 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": "7527aeb7-8912-404d-afb7-8c692c84422b", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321", "197322", "308047", "308048"], "spl_set_id": ["d2fd0b3e-9b78-44d0-82a6-96d6c6238750"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65862-676-01)", "package_ndc": "65862-676-01", "marketing_start_date": "20150731"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (65862-676-05)", "package_ndc": "65862-676-05", "marketing_start_date": "20150731"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65862-676-99)", "package_ndc": "65862-676-99", "marketing_start_date": "20150731"}], "brand_name": "Alprazolam", "product_id": "65862-676_7527aeb7-8912-404d-afb7-8c692c84422b", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "65862-676", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": ".25 mg/1"}], "application_number": "ANDA203346", "marketing_category": "ANDA", "marketing_start_date": "20150731", "listing_expiration_date": "20261231"}