Package 63304-090-05

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 63304-090-05
Digits Only 6330409005
Product NDC 63304-090
Product ID 63304-090_0e920885-4086-c99c-e063-6294a90aaa67
Description

500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-090-05)

Marketing

Marketing Status
Marketed Since 2020-01-02
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

POTASSIUM CHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0e920885-4086-c99c-e063-6294a90aaa67", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312504", "315183"], "spl_set_id": ["4d90d03d-7f0e-4d49-9e80-628dbc7165c0"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-090-01)", "package_ndc": "63304-090-01", "marketing_start_date": "20200102"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-090-05)", "package_ndc": "63304-090-05", "marketing_start_date": "20200102"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "63304-090_0e920885-4086-c99c-e063-6294a90aaa67", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "63304-090", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA208864", "marketing_category": "ANDA", "marketing_start_date": "20200102", "listing_expiration_date": "20261231"}