NDC 71335-0949 Baclofen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 71335-0949-0
Package Description: 120 TABLET in 1 BOTTLE
NDC Code 71335-0949-1
Package Description: 90 TABLET in 1 BOTTLE
NDC Code 71335-0949-2
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 71335-0949-3
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 71335-0949-4
Package Description: 45 TABLET in 1 BOTTLE
NDC Code 71335-0949-5
Package Description: 112 TABLET in 1 BOTTLE
NDC Code 71335-0949-6
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 71335-0949-7
Package Description: 56 TABLET in 1 BOTTLE
NDC Code 71335-0949-8
Package Description: 15 TABLET in 1 BOTTLE
NDC Code 71335-0949-9
Package Description: 84 TABLET in 1 BOTTLE
Product Details
What is NDC 71335-0949?
What are the uses for Baclofen?
Which are Baclofen UNII Codes?
The UNII codes for the active ingredients in this product are:
- BACLOFEN (UNII: H789N3FKE8)
- BACLOFEN (UNII: H789N3FKE8) (Active Moiety)
Which are Baclofen 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
What is the NDC to RxNorm Crosswalk for Baclofen?
- RxCUI: 197392 - baclofen 20 MG Oral Tablet
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Patient Education
Baclofen
Baclofen is used to treat pain and certain types of spasticity (muscle stiffness and tightness) from multiple sclerosis, spinal cord injuries, or other spinal cord diseases. Baclofen is in a class of medications called skeletal muscle relaxants. Baclofen acts on the spinal cord nerves and decreases the number and severity of muscle spasms caused by multiple sclerosis or spinal cord conditions. It also relieves pain and improves muscle movement.
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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".