Package 0338-0703-41

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 0338-0703-41
Digits Only 0338070341
Product NDC 0338-0703
Description

24 BAG in 1 CARTON (0338-0703-41) / 50 mL in 1 BAG

Marketing

Marketing Status
Marketed Since 1989-12-26
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "4cf18d0e-1854-48fb-b711-49b2a3042ae4", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312507", "1860239", "1860241", "1860463", "1860466"], "spl_set_id": ["092ddee4-572d-4771-8d95-880cea01097e"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BAG in 1 CARTON (0338-0703-41)  / 50 mL in 1 BAG", "package_ndc": "0338-0703-41", "marketing_start_date": "19891226"}, {"sample": false, "description": "24 BAG in 1 CARTON (0338-0703-48)  / 100 mL in 1 BAG", "package_ndc": "0338-0703-48", "marketing_start_date": "19891226"}], "brand_name": "Potassium Chloride", "product_id": "0338-0703_4cf18d0e-1854-48fb-b711-49b2a3042ae4", "dosage_form": "INJECTION, SOLUTION", "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": "0338-0703", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "29.8 g/1000mL"}], "application_number": "NDA019904", "marketing_category": "NDA", "marketing_start_date": "19891226", "listing_expiration_date": "20271231"}