Dopamine Hcl

   
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Dopamine Hcl


Drug - Dopamine 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) - Dopamine Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 40MG/ML
The potency of the active ingredient(s), Dopamine Hydrochloride. May repeat for multiple part products.

Applicant - SMITH AND NEPHEW
The firm name holding legal responsibility for Dopamine Hcl. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 070011
The FDA assigned number to Dopamine Hcl. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Dopamine Hcl. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

Therapeutic Equivalence (TE) Code -
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.

Approval Date - Aug 29, 1985
The date Dopamine 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 Dopamine Hcl. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.

Type - DISCN
The group or category of approved drugs Dopamine Hcl is in. Format is RX, OTC, DISCN.

Applicant Full Name - Smith And Nephew Solopak Div Smith And Nephew
The full name of the firm holding legal responsibility for the new application of Dopamine Hcl.

Dopamine Hcl