alprazolam

Generic: alprazolam

Labeler: asclemed usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name alprazolam
Generic Name alprazolam
Labeler asclemed usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alprazolam .25 mg/1

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-664
Product ID 76420-664_0ea9692e-7d75-80f3-e063-6294a90ad6f9
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 76420664
Hyphenated Format 76420-664

Supplemental Identifiers

RxCUI
197321 197322 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
  • 100 TABLET in 1 BOTTLE (76420-664-01)
  • 30 TABLET in 1 BOTTLE (76420-664-30)
  • 60 TABLET in 1 BOTTLE (76420-664-60)
  • 90 TABLET in 1 BOTTLE (76420-664-90)
source: ndc

Packages (4)

76420-664-01 100 TABLET in 1 BOTTLE (76420-664-01) 76420-664-30 30 TABLET in 1 BOTTLE (76420-664-30) 76420-664-60 60 TABLET in 1 BOTTLE (76420-664-60) 76420-664-90 90 TABLET in 1 BOTTLE (76420-664-90)

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": "0ea9692e-7d75-80f3-e063-6294a90ad6f9", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321", "197322", "308047", "308048"], "spl_set_id": ["e3245259-024f-4bd9-9ec6-94aa11febfd7"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-664-01)", "package_ndc": "76420-664-01", "marketing_start_date": "20240111"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-664-30)", "package_ndc": "76420-664-30", "marketing_start_date": "20240111"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-664-60)", "package_ndc": "76420-664-60", "marketing_start_date": "20240111"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-664-90)", "package_ndc": "76420-664-90", "marketing_start_date": "20240111"}], "brand_name": "Alprazolam", "product_id": "76420-664_0ea9692e-7d75-80f3-e063-6294a90ad6f9", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "76420-664", "dea_schedule": "CIV", "generic_name": "alprazolam", "labeler_name": "Asclemed USA, Inc.", "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"}