alendronate sodium

Generic: alendronate sodium

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alendronate sodium
Generic Name alendronate sodium
Labeler rising pharma holdings, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alendronate sodium 35 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 64980-341
Product ID 64980-341_3f943241-8c1a-4261-a337-f2fc45ad2835
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 64980341
Hyphenated Format 64980-341

Supplemental Identifiers

RxCUI
904396 904419 904431
UPC
0364980340038 0364980342148 0364980342018 0364980340014
UNII
2UY4M2U3RA

Packaging Origin

Original Packager
true

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
  • 35 mg/1
source: ndc
Packaging
  • 3 BLISTER PACK in 1 CARTON (64980-341-12) / 4 TABLET in 1 BLISTER PACK
  • 1 BLISTER PACK in 1 CARTON (64980-341-14) / 4 TABLET in 1 BLISTER PACK
source: ndc

Packages (2)

64980-341-12 3 BLISTER PACK in 1 CARTON (64980-341-12) / 4 TABLET in 1 BLISTER PACK 64980-341-14 1 BLISTER PACK in 1 CARTON (64980-341-14) / 4 TABLET in 1 BLISTER PACK

Ingredients (1)

alendronate sodium (35 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": "3f943241-8c1a-4261-a337-f2fc45ad2835", "openfda": {"upc": ["0364980340038", "0364980342148", "0364980342018", "0364980340014"], "unii": ["2UY4M2U3RA"], "rxcui": ["904396", "904419", "904431"], "spl_set_id": ["ffdd2496-d253-419b-85a6-8c615f7545f1"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (64980-341-12)  / 4 TABLET in 1 BLISTER PACK", "package_ndc": "64980-341-12", "marketing_start_date": "20080804"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (64980-341-14)  / 4 TABLET in 1 BLISTER PACK", "package_ndc": "64980-341-14", "marketing_start_date": "20080804"}], "brand_name": "Alendronate Sodium", "product_id": "64980-341_3f943241-8c1a-4261-a337-f2fc45ad2835", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "64980-341", "generic_name": "Alendronate Sodium", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alendronate Sodium", "active_ingredients": [{"name": "ALENDRONATE SODIUM", "strength": "35 mg/1"}], "application_number": "ANDA090124", "marketing_category": "ANDA", "marketing_start_date": "20080804", "listing_expiration_date": "20261231"}