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Bucladin-sDrug - Bucladin-s The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Buclizine Hydrochloride
Strength -
50MG
Applicant -
STUART PHARMS
New Drug Application (NDA) Number -
010911
Product Number -
006
Therapeutic Equivalence (TE) Code -
Approval Date -
Approved Prior to Jan 1, 1982
Reference Listed Drug (RLD) -
No
Type -
DISCN
Applicant Full Name -
Stuart Pharmaceuticals Div Ici Americas
Bucladin-s
Biphetap 4mg/5ml;25mg/5ml Elixir; Oral
Bromanate 4mg/5ml;25mg/5ml Elixir; Oral Dimetapp 2mg/5ml;12.5mg/5ml Elixir; Oral Bromatapp 12mg;75mg Tablet, Extended Release; Oral Dimetapp 12mg;75mg Tablet, Extended Release; Oral Efidac 24 Pseudoephedrine Hcl/brompheniramine Maleate 16mg;240mg Tablet, Extended Release; Oral Bucladin-s 50mg Tablet; Oral Bromfed-dm 2mg/5ml;10mg/5ml;30mg/5ml Syrup; Oral Dimetane-dx 2mg/5ml;10mg/5ml;30mg/5ml Syrup; Oral Myphetane Dx 2mg/5ml;10mg/5ml;30mg/5ml Syrup; Oral NewDrugInformation |