NDC 58118-0096 Venlafaxine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58118 - Clinical Solutions Wholesale, Llc
- 58118-0096 - Venlafaxine Hydrochloride
Product Characteristics
BROWN (C48332 - BUFF)
19 MM
93;7385;93;7385
Product Packages
NDC Code 58118-0096-8
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
Product Details
What is NDC 58118-0096?
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:
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- DIBUTYL SEBACATE (UNII: 4W5IH7FLNY)
- ETHYLCELLULOSE (7 MPA.S) (UNII: H3UP11403C)
- GELATIN (UNII: 2G86QN327L)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POVIDONE K30 (UNII: U725QWY32X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- SUCROSE (UNII: C151H8M554)
- STARCH, CORN (UNII: O8232NY3SJ)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
What is the NDC to RxNorm Crosswalk for Venlafaxine Hydrochloride?
- 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
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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".