NDC 42549-510 Diclofenac Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42549 - Stat Rx Usa Llc
- 42549-510 - Diclofenac Sodium
Product Characteristics
PINK (C48328 - LIGHT PINK)
G;DS;75
Product Packages
NDC Code 42549-510-30
Package Description: 30 TABLET, DELAYED RELEASE in 1 BOTTLE
NDC Code 42549-510-60
Package Description: 60 TABLET, DELAYED RELEASE in 1 BOTTLE
NDC Code 42549-510-90
Package Description: 90 TABLET, DELAYED RELEASE in 1 BOTTLE
Product Details
What is NDC 42549-510?
What are the uses for Diclofenac Sodium?
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:
- CROSPOVIDONE (UNII: 68401960MK)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHACRYLIC ACID (UNII: 1CS02G8656)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POVIDONE (UNII: FZ989GH94E)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
What is the NDC to RxNorm Crosswalk for Diclofenac Sodium?
- RxCUI: 855906 - diclofenac sodium 50 MG Delayed Release Oral Tablet
- RxCUI: 855926 - diclofenac sodium 75 MG Delayed Release Oral Tablet
* Please review the disclaimer below.
[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".