NDC Compounded Drug 72196-0202-1 Mannitol; Lidocaine Hydrochloride; Magnesium Sulfate Heptahydrate; Magnesium Chloride; Sodium Gluconate; Sodium Acetate; Potassium Chloride; Sodium Chloride; Sodium Bicarbonate
Solution Intracoronary
Compounded Drug Product Information
NDC Crossover Products Matching Mannitol; Lidocaine Hydrochloride; Magnesium Sulfate Heptahydrate; Magnesium Chloride; Sodium Gluconate; Sodium Acetate; Potassium Chloride; Sodium Chloride; Sodium Bicarbonate
NDC crossover of Del Nido Plasmalyte-a with NDC 72196-0202 a human compounded drug with other similar products matching the same substance name (Mannitol; Lidocaine Hydrochloride; Magnesium Sulfate Heptahydrate; Magnesium Chloride; Sodium Gluconate; Sodium Acetate; Potassium Chloride; Sodium Chloride; Sodium Bicarbonate) and the same administration route (intracoronary) or dosage form (solution).
NDC | Proprietary Name | Non-Proprietary Name | Package Desc | Dosage Form | Route Name | Company Name |
---|---|---|---|---|---|---|
71285-0202-1 | Del Nido Plasmalyte-a | Del Nido Plasmalyte-a | 1052.8 mL in 1 BAG | Solution | Intracoronary | Central Admixture Pharmacy Services, Inc. |
Frequently Asked Questions
What is the NDC number assigned to Del Nido Plasmalyte-a?
Del Nido Plasmalyte-a was assigned by its manufacturer with NDC product code 72196-0202. This product is a drug classified as a human compounded drug. Compounded drugs are medications created by combining or altering existing drugs to meet the specific needs of certain patients. The NDC directory only includes information about compounded drugs from facilities that choose to assign NDC numbers to their products.
Which are the NDC package codes for Del Nido Plasmalyte-a?
The NDC package code 72196-0202-1 was assigned to a 1052.8 mL in 1 BAG of mannitol; lidocaine hydrochloride; magnesium sulfate heptahydrate; magnesium chloride; sodium gluconate; sodium acetate; potassium chloride; sodium chloride; sodium bicarbonate administered intracoronary via solution.
Who manufactures this product?
Del Nido Plasmalyte-a is manufactured by an outsourced facility and labeled by Central Admixture Pharmacy Services, Inc.. All compounded drugs included in the NDC directory are classified as "Outsourcing Facility Compounded Human Drug Product (Exempt from Approval Requirements)". Outsourcing facilities are a type of drug compounding facility regulated under Section 503B of the FD&C Act could be eligible for exemptions from drug registration if they meet all the conditions specified under Section 503B.
Which are the NDC crossover matchings for this product?
We found 1 matching products that have the same substance, dosage form and administration route. The matching products are manufactured by Central Admixture Pharmacy Services, Inc. with NDC product codes 71285-0202-1.