alprazolam

Generic: alprazolam

Labeler: medsource pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

alprazolam .5 mg/1

Manufacturer
Medsource Pharmaceuticals

Identifiers & Regulatory

Product NDC 45865-257
Product ID 45865-257_1495f270-8125-14d2-e063-6294a90aff76
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 45865257
Hyphenated Format 45865-257

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 ANDA203346 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (45865-257-30)
source: ndc

Packages (1)

Ingredients (1)

alprazolam (.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1495f270-8125-14d2-e063-6294a90aff76", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["308048"], "spl_set_id": ["14960c0c-555f-acc1-e063-6394a90a232a"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Medsource Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (45865-257-30)", "package_ndc": "45865-257-30", "marketing_start_date": "20230515"}], "brand_name": "Alprazolam", "product_id": "45865-257_1495f270-8125-14d2-e063-6294a90aff76", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "45865-257", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "Medsource Pharmaceuticals", "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"}