Reglan

   
Google
 
Web NewDrugInformation.com

Reglan


Drug - Reglan
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) - Metoclopramide Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - EQ 10MG BASE
The potency of the active ingredient(s), Metoclopramide Hydrochloride. May repeat for multiple part products.

Applicant - SCHWARZ PHARMA
The firm name holding legal responsibility for Reglan. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 017854
The FDA assigned number to Reglan. Format is nnnnnn.

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

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

Approval Date - Approved Prior to Jan 1, 1982
The date Reglan 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) - Yes
The pioneer or innovator of Reglan. 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 Reglan is in. Format is RX, OTC, DISCN.

Applicant Full Name - Schwarz Pharma Inc
The full name of the firm holding legal responsibility for the new application of Reglan.

Reglan