NDC 50436-3250 Valacyclovir Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50436 - Unit Dose Services
- 50436-3250 - Valacyclovir Hydrochloride
Product Characteristics
23 MM
C3251000
2
Product Packages
NDC Code 50436-3250-1
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
NDC Code 50436-3250-3
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE
NDC Code 50436-3250-4
Package Description: 12 TABLET, FILM COATED in 1 BOTTLE
NDC Code 50436-3250-5
Package Description: 15 TABLET, FILM COATED in 1 BOTTLE
NDC Code 50436-3250-6
Package Description: 24 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 50436-3250?
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, UNSPECIFIED (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- 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
Pregabalin
Pregabalin capsules, oral solution (liquid), and extended-release (long-acting) tablets are used to relieve neuropathic pain (pain from damaged nerves) that can occur in your arms, hands, fingers, legs, feet, or toes if you have diabetes and postherpetic neuralgia (PHN; the burning, stabbing pain or aches that may last for months or years after an attack of shingles). Pregabalin capsules and oral solution are also used to relieve neuropathic pain that can occur after a spinal cord injury and to treat fibromyalgia (a long-lasting condition that may cause pain, muscle stiffness and tenderness, tiredness, and difficulty falling asleep or staying asleep). Pregabalin capsules and oral solution are used along with other medications to treat certain types of seizures in adults and children 1 month of age and older. Pregabalin is in a class of medications called anticonvulsants. It works by decreasing the number of pain signals that are sent out by damaged nerves in the body.
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* 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".