alprazolam

Generic: alprazolam

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alprazolam
Generic Name alprazolam
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alprazolam 2 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1894
Product ID 71335-1894_89f800b3-af12-4bcf-8328-fcba7deaf443
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 713351894
Hyphenated Format 71335-1894

Supplemental Identifiers

RxCUI
197322
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
  • 2 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1894-1)
  • 60 TABLET in 1 BOTTLE (71335-1894-2)
  • 90 TABLET in 1 BOTTLE (71335-1894-3)
  • 100 TABLET in 1 BOTTLE (71335-1894-4)
  • 10 TABLET in 1 BOTTLE (71335-1894-5)
  • 120 TABLET in 1 BOTTLE (71335-1894-6)
  • 40 TABLET in 1 BOTTLE (71335-1894-7)
source: ndc

Packages (7)

71335-1894-1 30 TABLET in 1 BOTTLE (71335-1894-1) 71335-1894-2 60 TABLET in 1 BOTTLE (71335-1894-2) 71335-1894-3 90 TABLET in 1 BOTTLE (71335-1894-3) 71335-1894-4 100 TABLET in 1 BOTTLE (71335-1894-4) 71335-1894-5 10 TABLET in 1 BOTTLE (71335-1894-5) 71335-1894-6 120 TABLET in 1 BOTTLE (71335-1894-6) 71335-1894-7 40 TABLET in 1 BOTTLE (71335-1894-7)

Ingredients (1)

alprazolam (2 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": "89f800b3-af12-4bcf-8328-fcba7deaf443", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["197322"], "spl_set_id": ["68d8b8d1-00a4-42c4-a796-90211fee1a6d"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1894-1)", "package_ndc": "71335-1894-1", "marketing_start_date": "20210629"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1894-2)", "package_ndc": "71335-1894-2", "marketing_start_date": "20210629"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1894-3)", "package_ndc": "71335-1894-3", "marketing_start_date": "20210629"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1894-4)", "package_ndc": "71335-1894-4", "marketing_start_date": "20210629"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-1894-5)", "package_ndc": "71335-1894-5", "marketing_start_date": "20210629"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-1894-6)", "package_ndc": "71335-1894-6", "marketing_start_date": "20210629"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71335-1894-7)", "package_ndc": "71335-1894-7", "marketing_start_date": "20210629"}], "brand_name": "Alprazolam", "product_id": "71335-1894_89f800b3-af12-4bcf-8328-fcba7deaf443", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "71335-1894", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": "2 mg/1"}], "application_number": "ANDA203346", "marketing_category": "ANDA", "marketing_start_date": "20150731", "listing_expiration_date": "20261231"}