NDC Compounded Drug 73198-122-30 Sodium Tetradecyl Sulfate
Injection, Solution Intravenous
Compounded Drug Product Information
NDC Crossover Products Matching Sodium Tetradecyl Sulfate
NDC crossover of Sodium Tetradecyl Sulfate 1.5% with NDC 73198-122 a human compounded drug with other similar products matching the same substance name (Sodium Tetradecyl Sulfate) and the same administration route (intravenous) or dosage form (injection, solution).
NDC | Proprietary Name | Non-Proprietary Name | Package Desc | Dosage Form | Route Name | Company Name |
---|---|---|---|---|---|---|
73198-120-30 | Sodium Tetradecyl Sulfate 0.1% | Sodium Tetradecyl Sulfate 0.1% | 30 mL in 1 VIAL, MULTI-DOSE | Injection, Solution | Intravenous | Olympia Pharmacy |
73198-120-30 | Sodium Tetradecyl Sulfate 0.1% | Sodium Tetradecyl Sulfate 0.1% | 30 mL in 1 VIAL, MULTI-DOSE | Injection, Solution | Intravenous | Olympia Pharmacy |
73198-121-30 | Sodium Tetradecyl Sulfate 0.3% | Sodium Tetradecyl Sulfate 0.3% | 30 mL in 1 VIAL, MULTI-DOSE | Injection, Solution | Intravenous | Olympia Pharmacy |
73198-121-30 | Sodium Tetradecyl Sulfate 0.3% | Sodium Tetradecyl Sulfate 0.3% | 30 mL in 1 VIAL, MULTI-DOSE | Injection, Solution | Intravenous | Olympia Pharmacy |
Frequently Asked Questions
What is the NDC number assigned to Sodium Tetradecyl Sulfate 0.3%?
Sodium Tetradecyl Sulfate 0.3% was assigned by its manufacturer with NDC product code 73198-122. 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 Sodium Tetradecyl Sulfate 0.3%?
The NDC package code 73198-122-30 was assigned to a 30 mL in 1 VIAL, MULTI-DOSE of sodium tetradecyl sulfate administered intravenous via injection, solution.
Who manufactures this product?
Sodium Tetradecyl Sulfate 0.3% is manufactured by an outsourced facility and labeled by Olympia Pharmacy. 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 4 matching products that have the same substance, dosage form and administration route. The matching products are manufactured by Olympia Pharmacy with NDC product codes 73198-120-30, 73198-120-30, 73198-121-30 and 73198-121-30.