NDC 50090-3880 Valacyclovir Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 50090-3880?
What are the uses for Valacyclovir Hydrochloride?
Which are Valacyclovir Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- VALACYCLOVIR HYDROCHLORIDE (UNII: G447S0T1VC)
- ACYCLOVIR (UNII: X4HES1O11F) (Active Moiety)
Which are Valacyclovir 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:
- CROSPOVIDONE (15 MPA.S AT 5%) (UNII: 68401960MK)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POVIDONE K90 (UNII: RDH86HJV5Z)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Valacyclovir Hydrochloride?
- RxCUI: 313564 - valACYclovir 1 GM Oral Tablet
- RxCUI: 313564 - valacyclovir 1000 MG Oral Tablet
- RxCUI: 313564 - valacyclovir (as valacyclovir HCl) 1 GM Oral Tablet
- RxCUI: 313564 - valacyclovir 1 GM Oral Tablet
- RxCUI: 313565 - valACYclovir 500 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Valacyclovir
Valacyclovir is used to treat herpes zoster (shingles) and genital herpes. It does not cure herpes infections but decreases pain and itching, helps sores to heal, and prevents new ones from forming. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
[Learn More]
* 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".