alendronate sodium

Generic: alendronate sodium

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alendronate sodium
Generic Name alendronate sodium
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alendronate sodium 70 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-048
Product ID 71205-048_6db7f218-1343-4b68-b72d-6605f1838e97
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090124
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 71205048
Hyphenated Format 71205-048

Supplemental Identifiers

RxCUI
904431
UPC
0371205048044
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 ANDA090124 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 70 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (71205-048-04) / 4 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

71205-048-04 1 BLISTER PACK in 1 CARTON (71205-048-04) / 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": "6db7f218-1343-4b68-b72d-6605f1838e97", "openfda": {"upc": ["0371205048044"], "unii": ["2UY4M2U3RA"], "rxcui": ["904431"], "spl_set_id": ["6c4d13fb-490c-4ea9-9b04-003c8d8e9f0c"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (71205-048-04)  / 4 TABLET in 1 BLISTER PACK", "package_ndc": "71205-048-04", "marketing_start_date": "20180601"}], "brand_name": "Alendronate Sodium", "product_id": "71205-048_6db7f218-1343-4b68-b72d-6605f1838e97", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "71205-048", "generic_name": "Alendronate Sodium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alendronate Sodium", "active_ingredients": [{"name": "ALENDRONATE SODIUM", "strength": "70 mg/1"}], "application_number": "ANDA090124", "marketing_category": "ANDA", "marketing_start_date": "20080804", "listing_expiration_date": "20261231"}