alprazolam

Generic: alprazolam

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alprazolam
Generic Name alprazolam
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alprazolam .5 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-313
Product ID 72789-313_40bb1fd8-e70f-47eb-e063-6394a90a74a8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074342
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 1993-10-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789313
Hyphenated Format 72789-313

Supplemental Identifiers

RxCUI
308048
UPC
0372789313900
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 ANDA074342 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/1
source: ndc
Packaging
  • 6 TABLET in 1 BOTTLE, PLASTIC (72789-313-06)
  • 30 TABLET in 1 BOTTLE, PLASTIC (72789-313-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (72789-313-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (72789-313-90)
source: ndc

Packages (4)

72789-313-06 6 TABLET in 1 BOTTLE, PLASTIC (72789-313-06) 72789-313-30 30 TABLET in 1 BOTTLE, PLASTIC (72789-313-30) 72789-313-60 60 TABLET in 1 BOTTLE, PLASTIC (72789-313-60) 72789-313-90 90 TABLET in 1 BOTTLE, PLASTIC (72789-313-90)

Ingredients (1)

alprazolam (.5 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": "40bb1fd8-e70f-47eb-e063-6394a90a74a8", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0372789313900"], "unii": ["YU55MQ3IZY"], "rxcui": ["308048"], "spl_set_id": ["5040e1ed-32d6-4757-a0ee-b8240f3e7cf5"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (72789-313-06)", "package_ndc": "72789-313-06", "marketing_start_date": "20240618"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-313-30)", "package_ndc": "72789-313-30", "marketing_start_date": "20230731"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-313-60)", "package_ndc": "72789-313-60", "marketing_start_date": "20230509"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-313-90)", "package_ndc": "72789-313-90", "marketing_start_date": "20230316"}], "brand_name": "Alprazolam", "product_id": "72789-313_40bb1fd8-e70f-47eb-e063-6394a90a74a8", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72789-313", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": ".5 mg/1"}], "application_number": "ANDA074342", "marketing_category": "ANDA", "marketing_start_date": "19931001", "listing_expiration_date": "20261231"}