alprazolam

Generic: alprazolam

Labeler: avpak
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alprazolam
Generic Name alprazolam
Labeler avpak
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alprazolam .25 mg/1

Manufacturer
AvPAK

Identifiers & Regulatory

Product NDC 50268-033
Product ID 50268-033_3fa15074-b724-8144-e063-6294a90a5c84
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203346
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2025-09-25

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50268033
Hyphenated Format 50268-033

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 ANDA203346 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .25 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 BOX (50268-033-15) / 1 TABLET in 1 BLISTER PACK (50268-033-11)
source: ndc

Packages (1)

Ingredients (1)

alprazolam (.25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3fa15074-b724-8144-e063-6294a90a5c84", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321", "308047", "308048"], "spl_set_id": ["3fa14fa4-45a7-6ef4-e063-6394a90a1dcd"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-033-15)  / 1 TABLET in 1 BLISTER PACK (50268-033-11)", "package_ndc": "50268-033-15", "marketing_start_date": "20250925"}], "brand_name": "Alprazolam", "product_id": "50268-033_3fa15074-b724-8144-e063-6294a90a5c84", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "50268-033", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "AvPAK", "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": "20250925", "listing_expiration_date": "20261231"}