Pregabalindrug info
pregabalin 20 MG/ML Oral Solution
What it is used for
1 INDICATIONS & USAGE Pregabalin is indicated for: Management of neuropathic pain associated with diabetic peripheral neuropathy Management of postherpetic neuralgia Adjunctive therapy for the treatment of partial-onset seizures in patients 1 month of age and older Management of fibromyalgia Management of neuropathic pain associated with spinal cord injury Pregabalin is indicated for: Neuropathic pain associated with diabetic peripheral neuropathy (DPN) Postherpetic neuralgia (PHN) Adjunctive therapy for the treatment of partial-onset seizures in patients 1 month of age and older Fibromyalgia Neuropathic pain associated with spinal cord injury
Text above is quoted in full from the FDA-approved drug label published by openFDA, effective December 22, 2025. Matched to this product by RxNorm code. Cross-references to other sections of the full prescribing information have been removed, since they point to a document not shown here. Nothing else is changed: no sentence is shortened, reworded or summarised.
Description
Pregabalin is described chemically as ( S )-3-(aminomethyl)-5-methylhexanoic acid. The molecular formula is C 8 H 17 NO 2 and the molecular weight is 159.23. The chemical structure of pregabalin is: Pregabalin is a white to off-white, crystalline powder with a pKa1 of 4.2 and a pKa2 of 10.6. It is sparingly soluble in water. The log of the partition coefficient (n-octanol/0.05M phosphate buffer) at pH 7.4 is – 1.35. Pregabalin oral solution, 20 mg/mL, is administered orally and is supplied as a clear, colorless transparent solution contained in a 16 fluid ounce white HDPE bottle with a polyethylene-lined closure.The oral solution contains 20 mg/mL of pregabalin, along with cherry flavour,disodium hydrogen phosphate anhydrous, methylparaben, monobasic sodium phosphate anhydrous, propylparaben, purified water and sucralose micronized as inactive ingredients. pregabalin-structure
Text above is quoted in full from the FDA-approved drug label published by openFDA, effective December 22, 2025. Matched to this product by RxNorm code. Cross-references to other sections of the full prescribing information have been removed, since they point to a document not shown here. Nothing else is changed: no sentence is shortened, reworded or summarised.
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