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UltivaDrug - Ultiva The trade name of the product as shown on the labeling.
Dosage -
INJECTABLE; INJECTION
Active Ingredient(s) -
Remifentanil Hydrochloride
Strength -
EQ 5MG BASE/VIAL
Applicant -
ABBOTT
New Drug Application (NDA) Number -
020630
Product Number -
003
Therapeutic Equivalence (TE) Code -
Approval Date -
Jul 12, 1996
Reference Listed Drug (RLD) -
Yes
Type -
RX
Applicant Full Name -
Abbott Laboratories
Ultiva
Ultiva Eq 1mg Base/vial Injectable; Injection
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