alendronate sodium

Generic: alendronate sodium

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alendronate sodium
Generic Name alendronate sodium
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alendronate sodium 70 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-4692
Product ID 50090-4692_789fd89e-ccc6-4b79-9611-c35fa3061ba7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076768
Listing Expiration 2026-12-31
Marketing Start 2008-08-04

Pharmacologic Class

Classes
bisphosphonate [epc] diphosphonates [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500904692
Hyphenated Format 50090-4692

Supplemental Identifiers

RxCUI
904431
UNII
2UY4M2U3RA

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 alendronate sodium (source: ndc)
Generic Name alendronate sodium (source: ndc)
Application Number ANDA076768 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 70 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (50090-4692-0) / 4 TABLET in 1 BLISTER PACK
  • 3 BLISTER PACK in 1 CARTON (50090-4692-1) / 4 TABLET in 1 BLISTER PACK
source: ndc

Packages (2)

50090-4692-0 1 BLISTER PACK in 1 CARTON (50090-4692-0) / 4 TABLET in 1 BLISTER PACK 50090-4692-1 3 BLISTER PACK in 1 CARTON (50090-4692-1) / 4 TABLET in 1 BLISTER PACK

Ingredients (1)

alendronate sodium (70 mg/1)

Linked Drug Pages (1)

ALENDRONATE SODIUM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "789fd89e-ccc6-4b79-9611-c35fa3061ba7", "openfda": {"unii": ["2UY4M2U3RA"], "rxcui": ["904431"], "spl_set_id": ["fe1dd324-eb02-4a73-97f5-9b77a7df10a7"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50090-4692-0)  / 4 TABLET in 1 BLISTER PACK", "package_ndc": "50090-4692-0", "marketing_start_date": "20191107"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (50090-4692-1)  / 4 TABLET in 1 BLISTER PACK", "package_ndc": "50090-4692-1", "marketing_start_date": "20191107"}], "brand_name": "ALENDRONATE SODIUM", "product_id": "50090-4692_789fd89e-ccc6-4b79-9611-c35fa3061ba7", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "50090-4692", "generic_name": "Alendronate sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALENDRONATE SODIUM", "active_ingredients": [{"name": "ALENDRONATE SODIUM", "strength": "70 mg/1"}], "application_number": "ANDA076768", "marketing_category": "ANDA", "marketing_start_date": "20080804", "listing_expiration_date": "20261231"}