Package 69097-893-93

Brand: sevelamer carbonate

Generic: sevelamer carbonate
NDC Package

Package Facts

Identity

Package NDC 69097-893-93
Digits Only 6909789393
Product NDC 69097-893
Product ID 69097-893_b4a439b7-08e8-4d1b-abea-f7976010d323
Description

270 TABLET, FILM COATED in 1 BOTTLE (69097-893-93)

Marketing

Marketing Status
Marketed Since 2017-10-26
Brand sevelamer carbonate
Generic sevelamer carbonate
Sample Package No

Linked Drug Pages (1)

Sevelamer carbonate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b4a439b7-08e8-4d1b-abea-f7976010d323", "openfda": {"unii": ["9YCX42I8IU"], "rxcui": ["749206"], "spl_set_id": ["f63450bd-d075-4810-a277-e8bc41e4a5af"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "270 TABLET, FILM COATED in 1 BOTTLE (69097-893-93)", "package_ndc": "69097-893-93", "marketing_start_date": "20171026"}], "brand_name": "Sevelamer carbonate", "product_id": "69097-893_b4a439b7-08e8-4d1b-abea-f7976010d323", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "69097-893", "generic_name": "SEVELAMER CARBONATE", "labeler_name": "Cipla USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevelamer carbonate", "active_ingredients": [{"name": "SEVELAMER CARBONATE", "strength": "800 mg/1"}], "application_number": "ANDA203860", "marketing_category": "ANDA", "marketing_start_date": "20171026", "listing_expiration_date": "20261231"}