Package 70748-173-26

Brand: sevelamer hydrochloride

Generic: sevelamer hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70748-173-26
Digits Only 7074817326
Product NDC 70748-173
Product ID 70748-173_cc130cfa-f3e5-460d-92a8-69cc0f958dd2
Description

180 TABLET in 1 BOTTLE (70748-173-26)

Marketing

Marketing Status
Marketed Since 2022-02-25
Brand sevelamer hydrochloride
Generic sevelamer hydrochloride
Sample Package No

Linked Drug Pages (1)

Sevelamer hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cc130cfa-f3e5-460d-92a8-69cc0f958dd2", "openfda": {"unii": ["GLS2PGI8QG"], "rxcui": ["857224"], "spl_set_id": ["a56c857e-bc39-484c-908d-f5957857efbb"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET in 1 BOTTLE (70748-173-26)", "package_ndc": "70748-173-26", "marketing_start_date": "20220225"}], "brand_name": "Sevelamer hydrochloride", "product_id": "70748-173_cc130cfa-f3e5-460d-92a8-69cc0f958dd2", "dosage_form": "TABLET", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "70748-173", "generic_name": "Sevelamer hydrochloride", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevelamer hydrochloride", "active_ingredients": [{"name": "SEVELAMER HYDROCHLORIDE", "strength": "800 mg/1"}], "application_number": "ANDA213145", "marketing_category": "ANDA", "marketing_start_date": "20220225", "listing_expiration_date": "20261231"}