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 .5 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-035
Product ID 82804-035_68e6ef8c-4104-4636-9719-6aa386c892d9
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 82804035
Hyphenated Format 82804-035

Supplemental Identifiers

RxCUI
308048
UPC
0382804035304
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 ANDA203346 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (82804-035-30)
  • 60 TABLET in 1 BOTTLE (82804-035-60)
  • 90 TABLET in 1 BOTTLE (82804-035-90)
source: ndc

Packages (3)

82804-035-30 30 TABLET in 1 BOTTLE (82804-035-30) 82804-035-60 60 TABLET in 1 BOTTLE (82804-035-60) 82804-035-90 90 TABLET in 1 BOTTLE (82804-035-90)

Ingredients (1)

alprazolam (.5 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": "68e6ef8c-4104-4636-9719-6aa386c892d9", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0382804035304"], "unii": ["YU55MQ3IZY"], "rxcui": ["308048"], "spl_set_id": ["68e6ef8c-4104-4636-9719-6aa386c892d9"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-035-30)", "package_ndc": "82804-035-30", "marketing_start_date": "20231026"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (82804-035-60)", "package_ndc": "82804-035-60", "marketing_start_date": "20231026"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-035-90)", "package_ndc": "82804-035-90", "marketing_start_date": "20231026"}], "brand_name": "Alprazolam", "product_id": "82804-035_68e6ef8c-4104-4636-9719-6aa386c892d9", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "82804-035", "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": ".5 mg/1"}], "application_number": "ANDA203346", "marketing_category": "ANDA", "marketing_start_date": "20150731", "listing_expiration_date": "20261231"}