alendronate sodium

Generic: alendronate sodium

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

Drug Facts

Product Profile

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

alendronate sodium 70 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-7130
Product ID 68788-7130_e88fb31d-cfc6-4e20-95fa-90fa26bf8644
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076768
Listing Expiration 2027-12-31
Marketing Start 2018-03-30

Pharmacologic Class

Classes
bisphosphonate [epc] diphosphonates [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887130
Hyphenated Format 68788-7130

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
  • 4 TABLET in 1 BLISTER PACK (68788-7130-4)
source: ndc

Packages (1)

68788-7130-4 4 TABLET in 1 BLISTER PACK (68788-7130-4)

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": "e88fb31d-cfc6-4e20-95fa-90fa26bf8644", "openfda": {"unii": ["2UY4M2U3RA"], "rxcui": ["904431"], "spl_set_id": ["83e3ba94-d882-4b5c-87cb-af1eb0997efc"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET in 1 BLISTER PACK (68788-7130-4)", "package_ndc": "68788-7130-4", "marketing_start_date": "20180330"}], "brand_name": "ALENDRONATE SODIUM", "product_id": "68788-7130_e88fb31d-cfc6-4e20-95fa-90fa26bf8644", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "68788-7130", "generic_name": "Alendronate sodium", "labeler_name": "Preferred Pharmaceuticals 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": "20180330", "listing_expiration_date": "20271231"}