Meclizine Hcl

   
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Meclizine Hcl


Drug - Meclizine Hcl
The trade name of the product as shown on the labeling.

Dosage - TABLET; ORAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Meclizine Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 12.5MG
The potency of the active ingredient(s), Meclizine Hydrochloride. May repeat for multiple part products.

Applicant - PLIVA
The firm name holding legal responsibility for Meclizine Hcl. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 088732
The FDA assigned number to Meclizine Hcl. Format is nnnnnn.

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

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

Approval Date - Dec 11, 1985
The date Meclizine 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 Meclizine 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 Meclizine Hcl is in. Format is RX, OTC, DISCN.

Applicant Full Name - Pliva Inc
The full name of the firm holding legal responsibility for the new application of Meclizine Hcl.

Meclizine Hcl