NDC 43353-689 Venlafaxine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43353 - Aphena Pharma Solutions - Tennessee, Llc
- 43353-689 - Venlafaxine Hydrochloride
Product Characteristics
Product Packages
NDC Code 43353-689-53
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 43353-689?
What are the uses for Venlafaxine Hydrochloride?
Which are Venlafaxine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- VENLAFAXINE HYDROCHLORIDE (UNII: 7D7RX5A8MO)
- VENLAFAXINE (UNII: GRZ5RCB1QG) (Active Moiety)
Which are Venlafaxine Hydrochloride 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
What is the NDC to RxNorm Crosswalk for Venlafaxine Hydrochloride?
- RxCUI: 313584 - venlafaxine HCl 37.5 MG Oral Tablet
- RxCUI: 313584 - venlafaxine 37.5 MG Oral Tablet
- RxCUI: 313584 - venlafaxine 37.5 MG (as venlafaxine hydrochloride 42.5 MG) Oral Tablet
- RxCUI: 313586 - venlafaxine HCl 75 MG Oral Tablet
- RxCUI: 313586 - venlafaxine 75 MG Oral Tablet
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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".