Package 0641-0497-25
Brand: sodium chloride
Generic: sodium chloridePackage Facts
Identity
Package NDC
0641-0497-25
Digits Only
0641049725
Product NDC
0641-0497
Description
25 VIAL in 1 CARTON (0641-0497-25) / 2 mL in 1 VIAL (0641-0497-17)
Marketing
Marketing Status
Brand
sodium chloride
Generic
sodium chloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "0950e98d-bfec-40e8-9f56-ba90e0d6e8c8", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807636", "1807637"], "spl_set_id": ["e5ee8caa-b6ca-45ba-98fb-8305e6282141"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0641-0497-25) / 2 mL in 1 VIAL (0641-0497-17)", "package_ndc": "0641-0497-25", "marketing_start_date": "20130924"}], "brand_name": "Sodium Chloride", "product_id": "0641-0497_0950e98d-bfec-40e8-9f56-ba90e0d6e8c8", "dosage_form": "INJECTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0641-0497", "generic_name": "Sodium Chloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "9 mg/mL"}], "application_number": "ANDA201833", "marketing_category": "ANDA", "marketing_start_date": "20130924", "listing_expiration_date": "20261231"}