Trimethobenzamide Hcl
Drug - Trimethobenzamide Hcl
The trade name of the product as shown on the labeling.
Dosage -
INJECTABLE; INJECTION
The product dosage form and route separated by a semi-colon.
Active Ingredient(s) -
Trimethobenzamide Hydrochloride
Multiple ingredients are in alphabetical order.
Strength -
100MG/ML
The potency of the active ingredient(s), Trimethobenzamide Hydrochloride. May repeat for multiple part products.
Applicant -
HOSPIRA
The firm name holding legal responsibility for Trimethobenzamide Hcl. The firm name is condensed to a maximum twenty character unique string.
New Drug Application (NDA) Number -
088804
The FDA assigned number to Trimethobenzamide Hcl. Format is nnnnnn.
Product Number -
001
The FDA assigned number to identify Trimethobenzamide Hcl. Each strength is a separate product. May repeat for multiple part products. Format is nnn.
Therapeutic Equivalence (TE) Code -
AP
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.
Approval Date -
Apr 3, 1987
The date Trimethobenzamide Hcl was approved as stated in the FDA approval letter to the applicant. The format is Mmm dd, yyyy. Products approved prior to the January 1, 1982 contain the phrase: "Approved prior to Jan 1, 1982".
Reference Listed Drug (RLD) -
No
The pioneer or innovator of Trimethobenzamide Hcl. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.
Type -
RX
The group or category of approved drugs Trimethobenzamide Hcl is in. Format is RX, OTC, DISCN.
Applicant Full Name -
Hospira Inc
The full name of the firm holding legal responsibility for the new application of Trimethobenzamide Hcl.
Trimethobenzamide Hcl
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