alendronate sodium

Generic: alendronate sodium

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alendronate sodium
Generic Name alendronate sodium
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alendronate sodium 70 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-0033
Product ID 70518-0033_47d221be-7385-f815-e063-6294a90a15df
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076768
Listing Expiration 2027-12-31
Marketing Start 2016-12-01

Pharmacologic Class

Classes
bisphosphonate [epc] diphosphonates [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705180033
Hyphenated Format 70518-0033

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
  • 12 TABLET in 1 BLISTER PACK (70518-0033-0)
source: ndc

Packages (1)

70518-0033-0 12 TABLET in 1 BLISTER PACK (70518-0033-0)

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": "47d221be-7385-f815-e063-6294a90a15df", "openfda": {"unii": ["2UY4M2U3RA"], "rxcui": ["904431"], "spl_set_id": ["c4358ba7-1bf8-4b0a-9407-5ac279d04555"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BLISTER PACK (70518-0033-0)", "package_ndc": "70518-0033-0", "marketing_start_date": "20161201"}], "brand_name": "ALENDRONATE SODIUM", "product_id": "70518-0033_47d221be-7385-f815-e063-6294a90a15df", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "70518-0033", "generic_name": "Alendronate sodium", "labeler_name": "REMEDYREPACK INC.", "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": "20161201", "listing_expiration_date": "20271231"}