NDC 59923-602 Pamidronate Disodium
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What is NDC 59923-602?
What are the uses for Pamidronate Disodium?
Which are Pamidronate Disodium UNII Codes?
The UNII codes for the active ingredients in this product are:
- PAMIDRONATE DISODIUM (UNII: 8742T8ZQZA)
- PAMIDRONIC ACID (UNII: OYY3447OMC) (Active Moiety)
Which are Pamidronate Disodium Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- MANNITOL (UNII: 3OWL53L36A)
- WATER (UNII: 059QF0KO0R)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
What is the NDC to RxNorm Crosswalk for Pamidronate Disodium?
- RxCUI: 1737457 - pamidronate disodium 60 MG Injection
- RxCUI: 1737459 - pamidronate disodium 30 MG Injection
- RxCUI: 1737461 - pamidronate disodium 90 MG Injection
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Patient Education
Pamidronate Injection
Pamidronate is used to treat high levels of calcium in the blood that may be caused by certain types of cancer. Pamidronate is also used along with cancer chemotherapy to treat bone damage caused by multiple myeloma (cancer that begins in the plasma cells [a type of white blood cell that produces substances needed to fight infection]) or by breast cancer that has spread to the bones. Pamidronate is also used to treat Paget's disease (a condition in which the bones are soft and weak and may be deformed, painful, or easily broken). Pamidronate injection is in a class of medications called bisphosphonates. It works by slowing bone breakdown, increasing bone density (thickness) and decreasing the amount of calcium released from the bones into the blood.
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".