NDC 0115-1483 Diclofenac Sodium
NDC Code 0115-1483-56
Package Description: 1 TUBE in 1 CARTON / 50 g in 1 TUBE
NDC Code 0115-1483-61
Package Description: 1 TUBE in 1 CARTON / 100 g in 1 TUBE
Price per Unit: $0.39099 per GM
What is NDC 0115-1483?
The NDC code 0115-1483 is assigned by the FDA to the product Diclofenac Sodium which is a human prescription drug product labeled by Amneal Pharmaceuticals Of New York Llc. The product's dosage form is gel and is administered via topical form. The product is distributed in 2 packages with assigned NDC codes 0115-1483-56 1 tube in 1 carton / 50 g in 1 tube, 0115-1483-61 1 tube in 1 carton / 100 g in 1 tube. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.
What are the uses for Diclofenac Sodium?
Diclofenac is used to relieve pain, swelling (inflammation), and joint stiffness caused by arthritis. Reducing these symptoms helps you do more of your normal daily activities. This medication is known as a nonsteroidal anti-inflammatory drug (NSAID). If you are treating a chronic condition such as arthritis, ask your doctor about non-drug treatments and/or using other medications to treat your pain. See also Warning section.
What are Diclofenac Sodium Active Ingredients?
An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
- DICLOFENAC SODIUM 30 mg/g - A non-steroidal anti-inflammatory agent (NSAID) with antipyretic and analgesic actions. It is primarily available as the sodium salt.
Which are Diclofenac Sodium UNII Codes?
The UNII codes for the active ingredients in this product are:
- DICLOFENAC SODIUM (UNII: QTG126297Q)
- DICLOFENAC (UNII: 144O8QL0L1) (Active Moiety)
Which are Diclofenac Sodium 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:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- HYDROXYETHYL CELLULOSE (5000 CPS AT 1%) (UNII: X70SE62ZAR)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- WATER (UNII: 059QF0KO0R)
- PEG-7 METHYL ETHER (UNII: ENK4Y6S66X)
What is the NDC to RxNorm Crosswalk for Diclofenac Sodium?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
- RxCUI: 855642 - diclofenac sodium 3 % Topical Gel
- RxCUI: 855642 - diclofenac sodium 0.03 MG/MG Topical Gel
Which are the Pharmacologic Classes for Diclofenac Sodium?
A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.
* Please review the disclaimer below.
Diclofenac Topical (actinic keratosis)
Diclofenac topical gel (Solaraze) is used to treat actinic keratosis (flat, scaly growths on the skin caused by too much sun exposure). Diclofenac is in a class of medications called nonsteroidal anti-inflammatory drugs (NSAIDs). The way diclofenac gel works to treat actinic keratosis is not known. Diclofenac is also available as a liquid (Pennsaid) and a gel (Voltaren) that are applied to the skin to treat arthritis pain. This monograph only gives information about diclofenac gel (Solaraze) for actinic keratosis. If you are using either of the products for osteoarthritis, read the monograph entitled diclofenac topical (osteoarthritis pain).
* Please review the disclaimer below.
We have moved the product label and warning information to a dedicated page, please follow the link below:View Product Label