alendronate

Generic: alendronate sodium

Labeler: hangzhou minsheng binjiang pharmaceutical co., ltd.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alendronate
Generic Name alendronate sodium
Labeler hangzhou minsheng binjiang pharmaceutical co., ltd.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alendronate sodium 35 mg/1

Manufacturer
Hangzhou Minsheng Binjiang Pharmaceutical Co., Ltd.

Identifiers & Regulatory

Product NDC 60723-207
Product ID 60723-207_460d461d-4807-2ed0-e063-6394a90aad4a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090258
Listing Expiration 2026-12-31
Marketing Start 2017-12-05

Pharmacologic Class

Classes
bisphosphonate [epc] diphosphonates [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60723207
Hyphenated Format 60723-207

Supplemental Identifiers

RxCUI
904396 904431
UPC
0360723207330
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 (source: ndc)
Generic Name alendronate sodium (source: ndc)
Application Number ANDA090258 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 35 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (60723-207-31) / 4 TABLET in 1 BLISTER PACK
  • 3 BLISTER PACK in 1 CARTON (60723-207-32) / 4 TABLET in 1 BLISTER PACK
  • 2 BLISTER PACK in 1 CARTON (60723-207-33) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (3)

60723-207-31 1 BLISTER PACK in 1 CARTON (60723-207-31) / 4 TABLET in 1 BLISTER PACK 60723-207-32 3 BLISTER PACK in 1 CARTON (60723-207-32) / 4 TABLET in 1 BLISTER PACK 60723-207-33 2 BLISTER PACK in 1 CARTON (60723-207-33) / 10 TABLET in 1 BLISTER PACK

Ingredients (1)

alendronate sodium (35 mg/1)

Linked Drug Pages (1)

Alendronate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "460d461d-4807-2ed0-e063-6394a90aad4a", "openfda": {"upc": ["0360723207330"], "unii": ["2UY4M2U3RA"], "rxcui": ["904396", "904431"], "spl_set_id": ["a24fd39c-34a7-4de2-9439-781e612189ca"], "manufacturer_name": ["Hangzhou Minsheng Binjiang Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (60723-207-31)  / 4 TABLET in 1 BLISTER PACK", "package_ndc": "60723-207-31", "marketing_start_date": "20171205"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (60723-207-32)  / 4 TABLET in 1 BLISTER PACK", "package_ndc": "60723-207-32", "marketing_start_date": "20171205"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (60723-207-33)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "60723-207-33", "marketing_start_date": "20171205"}], "brand_name": "Alendronate", "product_id": "60723-207_460d461d-4807-2ed0-e063-6394a90aad4a", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "60723-207", "generic_name": "ALENDRONATE SODIUM", "labeler_name": "Hangzhou Minsheng Binjiang Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alendronate", "active_ingredients": [{"name": "ALENDRONATE SODIUM", "strength": "35 mg/1"}], "application_number": "ANDA090258", "marketing_category": "ANDA", "marketing_start_date": "20171205", "listing_expiration_date": "20261231"}