alprazolam

Generic: alprazolam

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alprazolam
Generic Name alprazolam
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alprazolam .5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5261
Product ID 50090-5261_01c5a0e6-1d41-4b4d-9413-d72d1d1834f6
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 500905261
Hyphenated Format 50090-5261

Supplemental Identifiers

RxCUI
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 ANDA207507 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-5261-0)
  • 20 TABLET in 1 BOTTLE (50090-5261-1)
  • 60 TABLET in 1 BOTTLE (50090-5261-2)
  • 90 TABLET in 1 BOTTLE (50090-5261-3)
source: ndc

Packages (4)

Ingredients (1)

alprazolam (.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "01c5a0e6-1d41-4b4d-9413-d72d1d1834f6", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["308048"], "spl_set_id": ["d2ff7095-ee9a-4034-854f-efcfec47b284"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-5261-0)", "package_ndc": "50090-5261-0", "marketing_start_date": "20201015"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (50090-5261-1)", "package_ndc": "50090-5261-1", "marketing_start_date": "20201015"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-5261-2)", "package_ndc": "50090-5261-2", "marketing_start_date": "20201015"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5261-3)", "package_ndc": "50090-5261-3", "marketing_start_date": "20201015"}], "brand_name": "Alprazolam", "product_id": "50090-5261_01c5a0e6-1d41-4b4d-9413-d72d1d1834f6", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "50090-5261", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": ".5 mg/1"}], "application_number": "ANDA207507", "marketing_category": "ANDA", "marketing_start_date": "20180709", "listing_expiration_date": "20261231"}