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Amantadine HclDrug - Amantadine Hcl The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Amantadine Hydrochloride
Strength -
100MG
Applicant -
USL PHARMA
New Drug Application (NDA) Number -
076186
Product Number -
001
Therapeutic Equivalence (TE) Code -
AB
Approval Date -
Dec 16, 2002
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Usl Pharma Inc
Amantadine Hcl
Amantadine Hcl 50mg/5ml Syrup; Oral
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