Package 63323-967-30

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 63323-967-30
Digits Only 6332396730
Product NDC 63323-967
Product ID 63323-967_a1b31b46-2bb4-457e-a30b-e7dab47a2c54
Description

25 VIAL, MULTI-DOSE in 1 TRAY (63323-967-30) / 30 mL in 1 VIAL, MULTI-DOSE (63323-967-01)

Marketing

Marketing Status
Marketed Since 2000-09-05
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": ["INTRAVENOUS"], "spl_id": "a1b31b46-2bb4-457e-a30b-e7dab47a2c54", "openfda": {"upc": ["0363323967017", "0363323965020", "0363323965013"], "unii": ["660YQ98I10"], "rxcui": ["204520", "1860132", "1860136", "1860139"], "spl_set_id": ["fcd4f458-ce27-417e-9bb6-de1cc49d44b9"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 TRAY (63323-967-30)  / 30 mL in 1 VIAL, MULTI-DOSE (63323-967-01)", "package_ndc": "63323-967-30", "marketing_start_date": "20000905"}], "brand_name": "Potassium Chloride", "product_id": "63323-967_a1b31b46-2bb4-457e-a30b-e7dab47a2c54", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "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": "63323-967", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "2 meq/mL"}], "application_number": "ANDA088908", "marketing_category": "ANDA", "marketing_start_date": "20000905", "listing_expiration_date": "20261231"}