NDC 43353-768 Simvastatin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43353 - Aphena Pharma Solutions - Tennessee, Inc.
- 43353-768 - Simvastatin
Product Characteristics
PINK (C48328 - DARK PINK TO PINK)
CAPSULE (C48336)
18 MM
B304;80
Product Packages
NDC Code 43353-768-15
Package Description: 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 43353-768?
What are the uses for Simvastatin?
Which are Simvastatin UNII Codes?
The UNII codes for the active ingredients in this product are:
- SIMVASTATIN (UNII: AGG2FN16EV)
- SIMVASTATIN (UNII: AGG2FN16EV) (Active Moiety)
Which are Simvastatin 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:
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- POVIDONE (UNII: FZ989GH94E)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
What is the NDC to RxNorm Crosswalk for Simvastatin?
- RxCUI: 200345 - simvastatin 80 MG Oral Tablet
- RxCUI: 312961 - simvastatin 20 MG 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".