alprazolam extended release (72162-1059)

Drug Facts

Product Profile

Brand Name alprazolam extended release

Generic Name alprazolam

Labeler bryant ranch prepack

Dosage Form TABLET, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

alprazolam .5 mg/1

Manufacturer

Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-1059

Product ID 72162-1059_6e4271db-f791-421e-8abd-65feddded931

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA078056

DEA Schedule civ

Listing Expiration 2026-12-31

Marketing Start 2007-03-12

Pharmacologic Class

Established (EPC)

benzodiazepine [epc]

Chemical Structure

benzodiazepines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721621059

Hyphenated Format 72162-1059

Supplemental Identifiers

RxCUI

433798

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 extended release (source: ndc)

Generic Name alprazolam (source: ndc)

Application Number ANDA078056 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

.5 mg/1

source: ndc

Packaging

45 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1059-2)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1059-3)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1059-6)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1059-9)

source: ndc

Packages (4)

72162-1059-2 45 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1059-2) 72162-1059-3 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1059-3) 72162-1059-6 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1059-6) 72162-1059-9 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1059-9)

Ingredients (1)

alprazolam (.5 mg/1)

Linked Drug Pages (1)

Alprazolam Extended Release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "6e4271db-f791-421e-8abd-65feddded931", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["433798"], "spl_set_id": ["4f6e4656-689f-46a6-a8ed-54ee55583357"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "45 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1059-2)", "package_ndc": "72162-1059-2", "marketing_start_date": "20230508"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1059-3)", "package_ndc": "72162-1059-3", "marketing_start_date": "20230508"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1059-6)", "package_ndc": "72162-1059-6", "marketing_start_date": "20230508"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1059-9)", "package_ndc": "72162-1059-9", "marketing_start_date": "20230508"}], "brand_name": "Alprazolam Extended Release", "product_id": "72162-1059_6e4271db-f791-421e-8abd-65feddded931", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72162-1059", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "brand_name_suffix": "Extended Release", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": ".5 mg/1"}], "application_number": "ANDA078056", "marketing_category": "ANDA", "marketing_start_date": "20070312", "listing_expiration_date": "20261231"}