alprazolam

Generic: alprazolam

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alprazolam
Generic Name alprazolam
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alprazolam .25 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-696
Product ID 71610-696_f27967d7-9517-4c95-81a2-29408e707f5a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074112
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 1995-12-29

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71610696
Hyphenated Format 71610-696

Supplemental Identifiers

RxCUI
308047
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 ANDA074112 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .25 mg/1
source: ndc
Packaging
  • 15 TABLET in 1 BOTTLE (71610-696-15)
  • 30 TABLET in 1 BOTTLE (71610-696-30)
  • 45 TABLET in 1 BOTTLE (71610-696-45)
  • 60 TABLET in 1 BOTTLE (71610-696-53)
  • 90 TABLET in 1 BOTTLE (71610-696-60)
  • 120 TABLET in 1 BOTTLE (71610-696-70)
source: ndc

Packages (6)

71610-696-15 15 TABLET in 1 BOTTLE (71610-696-15) 71610-696-30 30 TABLET in 1 BOTTLE (71610-696-30) 71610-696-45 45 TABLET in 1 BOTTLE (71610-696-45) 71610-696-53 60 TABLET in 1 BOTTLE (71610-696-53) 71610-696-60 90 TABLET in 1 BOTTLE (71610-696-60) 71610-696-70 120 TABLET in 1 BOTTLE (71610-696-70)

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": "f27967d7-9517-4c95-81a2-29408e707f5a", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["308047"], "spl_set_id": ["54c790c5-2e6c-439d-8e3b-7502c962a596"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (71610-696-15)", "package_ndc": "71610-696-15", "marketing_start_date": "20230320"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71610-696-30)", "package_ndc": "71610-696-30", "marketing_start_date": "20230320"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (71610-696-45)", "package_ndc": "71610-696-45", "marketing_start_date": "20230320"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71610-696-53)", "package_ndc": "71610-696-53", "marketing_start_date": "20230320"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-696-60)", "package_ndc": "71610-696-60", "marketing_start_date": "20230320"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71610-696-70)", "package_ndc": "71610-696-70", "marketing_start_date": "20230320"}], "brand_name": "Alprazolam", "product_id": "71610-696_f27967d7-9517-4c95-81a2-29408e707f5a", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "71610-696", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": ".25 mg/1"}], "application_number": "ANDA074112", "marketing_category": "ANDA", "marketing_start_date": "19951229", "listing_expiration_date": "20261231"}