NDC Compounded Drug 70092-004-37 Amiodarone
Injection Intravenous
Compounded Drug Product Information
NDC Crossover Products Matching Amiodarone
NDC crossover of Amiodarone 450mg Add To 250ml D5w Ivb with NDC 70092-004 a human compounded drug with other similar products matching the same substance name (Amiodarone) and the same administration route (intravenous) or dosage form (injection).
NDC | Proprietary Name | Non-Proprietary Name | Package Desc | Dosage Form | Route Name | Company Name |
---|---|---|---|---|---|---|
70092-005-38 | Amiodarone 900mg Add To 500ml D5w Ivb | Amiodarone 900mg Add To 500ml D5w Ivb | 500 mL in 1 BAG | Injection | Parenteral | Quva Pharma, Inc. |
70092-005-38 | Amiodarone 900mg Add To 500ml D5w Ivb | Amiodarone 900mg Add To 500ml D5w Ivb | 500 mL in 1 BAG | Injection | Intravenous | Quva Pharma, Inc. |
70092-005-38 | Amiodarone 900mg Add To 500ml D5w Ivb | Amiodarone 900mg Add To 500ml D5w Ivb | 500 mL in 1 BAG | Injection | Intravenous | Quva Pharma, Inc. |
70092-005-38 | Amiodarone 900mg Add To 500ml D5w Ivb | Amiodarone 900mg Add To 500ml D5w Ivb | 500 mL in 1 BAG | Injection | Intravenous | Quva Pharma, Inc. |
Frequently Asked Questions
What is the NDC number assigned to Amiodarone 900mg Add To 500ml D5w Ivb?
Amiodarone 900mg Add To 500ml D5w Ivb was assigned by its manufacturer with NDC product code 70092-004. 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 Amiodarone 900mg Add To 500ml D5w Ivb?
The NDC package code 70092-004-37 was assigned to a 250 mL in 1 BAG of amiodarone administered intravenous via injection.
Who manufactures this product?
Amiodarone 900mg Add To 500ml D5w Ivb is manufactured by an outsourced facility and labeled by Quva Pharma, 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 4 matching products that have the same substance, dosage form and administration route. The matching products are manufactured by QuVa Pharma, Inc. with NDC product codes 70092-005-38, 70092-005-38, 70092-005-38 and 70092-005-38.