NDC 21695-045 Effexor Xr Extended-release
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-045 - Effexor
Product Characteristics
GRAY (C48324 - GRAY)
Product Packages
NDC Code 21695-045-15
Package Description: 15 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 21695-045?
What are the uses for Effexor Xr Extended-release?
Which are Effexor Xr Extended-release UNII Codes?
The UNII codes for the active ingredients in this product are:
- VENLAFAXINE HYDROCHLORIDE (UNII: 7D7RX5A8MO)
- VENLAFAXINE (UNII: GRZ5RCB1QG) (Active Moiety)
Which are Effexor Xr Extended-release 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:
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- ETHYLCELLULOSE (100 MPA.S) (UNII: 47MLB0F1MV)
- GELATIN (UNII: 2G86QN327L)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Effexor Xr Extended-release?
- RxCUI: 313581 - venlafaxine HCl 150 MG 24HR Extended Release Oral Capsule
- RxCUI: 313581 - 24 HR venlafaxine 150 MG Extended Release Oral Capsule
- RxCUI: 313581 - venlafaxine (as venlafaxine HCl) 150 MG 24 HR Extended Release Oral Capsule
- RxCUI: 313583 - venlafaxine HCl 37.5 MG 24HR Extended Release Oral Capsule
- RxCUI: 313583 - 24 HR venlafaxine 37.5 MG Extended Release Oral Capsule
* 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".