NDC 50436-3250 Valacyclovir Hydrochloride

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50436-3250
Proprietary Name:
Valacyclovir Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Unit Dose Services
Labeler Code:
50436
Start Marketing Date: [9]
04-05-2012
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333)
Shape:
CAPSULE (C48336)
Size(s):
18 MM
23 MM
Imprint(s):
C324500
C3251000
Score:
1
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?

The NDC code 50436-3250 is assigned by the FDA to the product Valacyclovir Hydrochloride which is product labeled by Unit Dose Services. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 50436-3250-1 30 tablet, film coated in 1 bottle , 50436-3250-3 90 tablet, film coated in 1 bottle , 50436-3250-4 12 tablet, film coated in 1 bottle , 50436-3250-5 15 tablet, film coated in 1 bottle , 50436-3250-6 24 tablet, film coated in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Valacyclovir Hydrochloride?

Valacyclovir hydrochloride is contraindicated in patients who have had a demonstrated clinically significant hypersensitivity reaction (e.g., anaphylaxis) to valacyclovir, acyclovir, or any component of the formulation [see Adverse Reactions (6.3)].

Which are Valacyclovir Hydrochloride UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

What is the NDC to RxNorm Crosswalk for Valacyclovir Hydrochloride?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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.
[Learn More]


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Product Footnotes

[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".