Package 0054-0282-59

Brand: alendronate sodium

Generic: alendronate sodium
NDC Package

Package Facts

Identity

Package NDC 0054-0282-59
Digits Only 0054028259
Product NDC 0054-0282
Product ID 0054-0282_56e063a8-8c3d-4445-91fd-0c8806c2b127
Description

4 BOTTLE, UNIT-DOSE in 1 CARTON (0054-0282-59) / 75 mL in 1 BOTTLE, UNIT-DOSE

Marketing

Marketing Status
Marketed Since 2020-10-30
Brand alendronate sodium
Generic alendronate sodium
Sample Package No

Linked Drug Pages (1)

Alendronate Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "56e063a8-8c3d-4445-91fd-0c8806c2b127", "openfda": {"upc": ["0300540282592"], "unii": ["2UY4M2U3RA"], "rxcui": ["904447"], "spl_set_id": ["c910bb05-279b-4ffa-a867-46f4a0853ed5"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BOTTLE, UNIT-DOSE in 1 CARTON (0054-0282-59)  / 75 mL in 1 BOTTLE, UNIT-DOSE", "package_ndc": "0054-0282-59", "marketing_start_date": "20201030"}], "brand_name": "Alendronate Sodium", "product_id": "0054-0282_56e063a8-8c3d-4445-91fd-0c8806c2b127", "dosage_form": "SOLUTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "0054-0282", "generic_name": "Alendronate Sodium", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alendronate Sodium", "active_ingredients": [{"name": "ALENDRONATE SODIUM", "strength": "70 mg/75mL"}], "application_number": "ANDA090520", "marketing_category": "ANDA", "marketing_start_date": "20201030", "listing_expiration_date": "20271231"}