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 1 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-2896
Product ID 50090-2896_71cb1809-575a-436e-be2f-2a457cd1a17d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074112
DEA Schedule civ
Marketing Start 1995-12-29
Marketing End 2027-03-19

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500902896
Hyphenated Format 50090-2896

Supplemental Identifiers

RxCUI
197321 197322 308047
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 ANDA074112 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-2896-1)
  • 60 TABLET in 1 BOTTLE (50090-2896-2)
  • 100 TABLET in 1 BOTTLE (50090-2896-3)
source: ndc

Packages (3)

50090-2896-1 30 TABLET in 1 BOTTLE (50090-2896-1) 50090-2896-2 60 TABLET in 1 BOTTLE (50090-2896-2) 50090-2896-3 100 TABLET in 1 BOTTLE (50090-2896-3)

Ingredients (1)

alprazolam (1 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": "71cb1809-575a-436e-be2f-2a457cd1a17d", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321", "197322", "308047"], "spl_set_id": ["3c0cb60f-1c3a-48a6-ad16-f14351548412"], "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 (50090-2896-1)", "package_ndc": "50090-2896-1", "marketing_end_date": "20270319", "marketing_start_date": "20170301"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-2896-2)", "package_ndc": "50090-2896-2", "marketing_end_date": "20270319", "marketing_start_date": "20230607"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-2896-3)", "package_ndc": "50090-2896-3", "marketing_end_date": "20270319", "marketing_start_date": "20230607"}], "brand_name": "Alprazolam", "product_id": "50090-2896_71cb1809-575a-436e-be2f-2a457cd1a17d", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "50090-2896", "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": "1 mg/1"}], "application_number": "ANDA074112", "marketing_category": "ANDA", "marketing_end_date": "20270319", "marketing_start_date": "19951229"}