alprazolam odt c-iv

Generic: alprazolam odt c-iv

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alprazolam odt c-iv
Generic Name alprazolam odt c-iv
Labeler direct_rx
Dosage Form TABLET, ORALLY DISINTEGRATING
Routes
ORAL
Active Ingredients

alprazolam .5 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-637
Product ID 72189-637_3cf95203-c8b5-9f06-e063-6394a90abc9c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078088
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2025-08-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189637
Hyphenated Format 72189-637

Supplemental Identifiers

RxCUI
485415
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 odt c-iv (source: ndc)
Generic Name alprazolam odt c-iv (source: ndc)
Application Number ANDA078088 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/1
source: ndc
Packaging
  • 2 TABLET, ORALLY DISINTEGRATING in 1 CARTON (72189-637-02)
source: ndc

Packages (1)

72189-637-02 2 TABLET, ORALLY DISINTEGRATING in 1 CARTON (72189-637-02)

Ingredients (1)

alprazolam (.5 mg/1)

Linked Drug Pages (1)

Alprazolam ODT C-IV ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3cf95203-c8b5-9f06-e063-6394a90abc9c", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["485415"], "spl_set_id": ["3cf95203-c8b4-9f06-e063-6394a90abc9c"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, ORALLY DISINTEGRATING in 1 CARTON (72189-637-02)", "package_ndc": "72189-637-02", "marketing_start_date": "20250822"}], "brand_name": "Alprazolam ODT C-IV", "product_id": "72189-637_3cf95203-c8b5-9f06-e063-6394a90abc9c", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72189-637", "dea_schedule": "CIV", "generic_name": "Alprazolam ODT C-IV", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam ODT C-IV", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": ".5 mg/1"}], "application_number": "ANDA078088", "marketing_category": "ANDA", "marketing_start_date": "20250822", "listing_expiration_date": "20261231"}