alprazolam

Generic: alprazolam

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC 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 67544-414
Product ID 67544-414_51152b89-539c-4c80-bb84-d7f2dc082953
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA018276
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 1981-10-16

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67544414
Hyphenated Format 67544-414

Supplemental Identifiers

RxCUI
197321 308047 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 NDA018276 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .25 mg/1
source: ndc
Packaging
  • 15 TABLET in 1 BOTTLE (67544-414-15)
  • 30 TABLET in 1 BOTTLE (67544-414-30)
  • 45 TABLET in 1 BOTTLE (67544-414-45)
  • 60 TABLET in 1 BOTTLE (67544-414-53)
  • 90 TABLET in 1 BOTTLE (67544-414-60)
  • 120 TABLET in 1 BOTTLE (67544-414-70)
  • 180 TABLET in 1 BOTTLE (67544-414-80)
source: ndc

Packages (7)

67544-414-15 15 TABLET in 1 BOTTLE (67544-414-15) 67544-414-30 30 TABLET in 1 BOTTLE (67544-414-30) 67544-414-45 45 TABLET in 1 BOTTLE (67544-414-45) 67544-414-53 60 TABLET in 1 BOTTLE (67544-414-53) 67544-414-60 90 TABLET in 1 BOTTLE (67544-414-60) 67544-414-70 120 TABLET in 1 BOTTLE (67544-414-70) 67544-414-80 180 TABLET in 1 BOTTLE (67544-414-80)

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": "51152b89-539c-4c80-bb84-d7f2dc082953", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321", "308047", "308048"], "spl_set_id": ["964d7f43-34a6-45af-a95f-3b9ade17c6a5"], "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 (67544-414-15)", "package_ndc": "67544-414-15", "marketing_start_date": "20060616"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (67544-414-30)", "package_ndc": "67544-414-30", "marketing_start_date": "20050630"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (67544-414-45)", "package_ndc": "67544-414-45", "marketing_start_date": "20060601"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (67544-414-53)", "package_ndc": "67544-414-53", "marketing_start_date": "20050630"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (67544-414-60)", "package_ndc": "67544-414-60", "marketing_start_date": "20050623"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (67544-414-70)", "package_ndc": "67544-414-70", "marketing_start_date": "20050907"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (67544-414-80)", "package_ndc": "67544-414-80", "marketing_start_date": "20080222"}], "brand_name": "Alprazolam", "product_id": "67544-414_51152b89-539c-4c80-bb84-d7f2dc082953", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "67544-414", "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": "NDA018276", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "19811016", "listing_expiration_date": "20261231"}