alprazolam

Generic: alprazolam

Labeler: sandoz inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

alprazolam 1 mg/1

Manufacturer
Sandoz Inc

Identifiers & Regulatory

Product NDC 0781-1079
Product ID 0781-1079_4c8c7366-aa3b-4124-9d64-67fb0ead6e15
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 07811079
Hyphenated Format 0781-1079

Supplemental Identifiers

RxCUI
197321 197322 308047 308048
UNII
YU55MQ3IZY
NUI
N0000175694 M0002356

Packaging Origin

Original Packager
true

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
  • 100 TABLET in 1 BOTTLE (0781-1079-01)
  • 500 TABLET in 1 BOTTLE (0781-1079-05)
  • 1000 TABLET in 1 BOTTLE (0781-1079-10)
source: ndc

Packages (3)

0781-1079-01 100 TABLET in 1 BOTTLE (0781-1079-01) 0781-1079-05 500 TABLET in 1 BOTTLE (0781-1079-05) 0781-1079-10 1000 TABLET in 1 BOTTLE (0781-1079-10)

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": "4c8c7366-aa3b-4124-9d64-67fb0ead6e15", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321", "197322", "308047", "308048"], "spl_set_id": ["d9b0e228-17cf-40d7-b62e-5050311c571c"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0781-1079-01)", "package_ndc": "0781-1079-01", "marketing_end_date": "20270319", "marketing_start_date": "19951229"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0781-1079-05)", "package_ndc": "0781-1079-05", "marketing_end_date": "20270319", "marketing_start_date": "19951229"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (0781-1079-10)", "package_ndc": "0781-1079-10", "marketing_end_date": "20270319", "marketing_start_date": "19951229"}], "brand_name": "Alprazolam", "product_id": "0781-1079_4c8c7366-aa3b-4124-9d64-67fb0ead6e15", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "0781-1079", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "Sandoz Inc", "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"}