Package 78206-135-01

Brand: fosamax

Generic: alendronate sodium
NDC Package

Package Facts

Identity

Package NDC 78206-135-01
Digits Only 7820613501
Product NDC 78206-135
Product ID 78206-135_9cc10d27-3960-41a0-9736-8fe902c6984f
Description

4 TABLET in 1 BLISTER PACK (78206-135-01)

Marketing

Marketing Status
Marketed Since 2021-06-01
Brand fosamax
Generic alendronate sodium
Sample Package No

Linked Drug Pages (1)

FOSAMAX ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9cc10d27-3960-41a0-9736-8fe902c6984f", "openfda": {"unii": ["2UY4M2U3RA"], "rxcui": ["904431", "904433"], "spl_set_id": ["14e931fd-2c5f-4d90-b7db-5980706f4a56"], "manufacturer_name": ["Organon LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET in 1 BLISTER PACK (78206-135-01)", "package_ndc": "78206-135-01", "marketing_start_date": "20210601"}], "brand_name": "FOSAMAX", "product_id": "78206-135_9cc10d27-3960-41a0-9736-8fe902c6984f", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "78206-135", "generic_name": "alendronate sodium", "labeler_name": "Organon LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FOSAMAX", "active_ingredients": [{"name": "ALENDRONATE SODIUM", "strength": "70 mg/1"}], "application_number": "NDA020560", "marketing_category": "NDA", "marketing_start_date": "20210601", "listing_expiration_date": "20271231"}