Package 76282-682-46
Brand: alendronate sodium
Generic: alendronate sodiumPackage Facts
Identity
Package NDC
76282-682-46
Digits Only
7628268246
Product NDC
76282-682
Description
3 BLISTER PACK in 1 CARTON (76282-682-46) / 4 TABLET in 1 BLISTER PACK (76282-682-45)
Marketing
Marketing Status
Brand
alendronate sodium
Generic
alendronate sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2012c7a8-8aa7-4c18-a8c3-fe74d74ac873", "openfda": {"unii": ["2UY4M2U3RA"], "rxcui": ["904396", "904431"], "spl_set_id": ["91a0f73a-d8cd-4197-b431-40707a2150b9"], "manufacturer_name": ["EXELAN PHARMACEUTICALS INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (76282-682-46) / 4 TABLET in 1 BLISTER PACK (76282-682-45)", "package_ndc": "76282-682-46", "marketing_start_date": "20210202"}], "brand_name": "ALENDRONATE SODIUM", "product_id": "76282-682_2012c7a8-8aa7-4c18-a8c3-fe74d74ac873", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "76282-682", "generic_name": "Alendronate sodium", "labeler_name": "EXELAN 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": "20210202", "listing_expiration_date": "20261231"}