Package 69097-967-93
Brand: sevelamer carbonate
Generic: sevelamer carbonatePackage Facts
Identity
Package NDC
69097-967-93
Digits Only
6909796793
Product NDC
69097-967
Description
270 TABLET, FILM COATED in 1 BOTTLE (69097-967-93)
Marketing
Marketing Status
Brand
sevelamer carbonate
Generic
sevelamer carbonate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "444a974f-7f31-4b53-93c9-f5b9a251f711", "openfda": {"upc": ["0369097967932"], "unii": ["9YCX42I8IU"], "rxcui": ["749206"], "spl_set_id": ["134f32c1-b5d5-44d0-9da5-85033e99320a"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "270 TABLET, FILM COATED in 1 BOTTLE (69097-967-93)", "package_ndc": "69097-967-93", "marketing_start_date": "20190808"}], "brand_name": "Sevelamer carbonate", "product_id": "69097-967_444a974f-7f31-4b53-93c9-f5b9a251f711", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "69097-967", "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"}