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
Routes
ORAL
Active Ingredients

alprazolam 1 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-227
Product ID 71205-227_c256eb0e-ff92-498d-9a9d-820b63126233
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207507
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2018-07-09

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205227
Hyphenated Format 71205-227

Supplemental Identifiers

RxCUI
197321
UPC
0371205227302
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 ANDA207507 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE (71205-227-10)
  • 30 TABLET in 1 BOTTLE (71205-227-30)
  • 60 TABLET in 1 BOTTLE (71205-227-60)
  • 90 TABLET in 1 BOTTLE (71205-227-90)
source: ndc

Packages (4)

71205-227-10 10 TABLET in 1 BOTTLE (71205-227-10) 71205-227-30 30 TABLET in 1 BOTTLE (71205-227-30) 71205-227-60 60 TABLET in 1 BOTTLE (71205-227-60) 71205-227-90 90 TABLET in 1 BOTTLE (71205-227-90)

Ingredients (1)

alprazolam (1 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": "c256eb0e-ff92-498d-9a9d-820b63126233", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0371205227302"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321"], "spl_set_id": ["2d04c305-70d6-4a99-8c82-720c5398a46c"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (71205-227-10)", "package_ndc": "71205-227-10", "marketing_start_date": "20221110"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-227-30)", "package_ndc": "71205-227-30", "marketing_start_date": "20190201"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-227-60)", "package_ndc": "71205-227-60", "marketing_start_date": "20190201"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-227-90)", "package_ndc": "71205-227-90", "marketing_start_date": "20190201"}], "brand_name": "Alprazolam", "product_id": "71205-227_c256eb0e-ff92-498d-9a9d-820b63126233", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "71205-227", "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": "ANDA207507", "marketing_category": "ANDA", "marketing_start_date": "20180709", "listing_expiration_date": "20261231"}