AMANTADINE HYDROCHLORIDE

Labeler
PAI Holdings, LLC dba PAI Pharma
Dosage Form
SOLUTION
Route
ORAL
NDCs
0121-0646-16, 0121-0646-10
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Active Ingredients

Display Name UNII Strength
Amantadine Hydrochloride M6Q1EO9TD0 50 mg/5 mL

Matched Sugar Alcohols

Substance UNII
Sorbitol 506T60A25R

Inactive Ingredients

Display Name UNII
Anhydrous Citric Acid XF417D3PSL
Methylparaben A2I8C7HI9T
Propylene Glycol 6DC9Q167V3
Propylparaben Z8IX2SC1OH
Water 059QF0KO0R
Sorbitol 506T60A25R
Sodium Hydroxide 55X04QC32I