Meclofenamate Sodium

   
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Meclofenamate Sodium


Drug - Meclofenamate Sodium
The trade name of the product as shown on the labeling.

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

Active Ingredient(s) - Meclofenamate Sodium
Multiple ingredients are in alphabetical order.

Strength - EQ 50MG BASE
The potency of the active ingredient(s), Meclofenamate Sodium. May repeat for multiple part products.

Applicant - WATSON LABS
The firm name holding legal responsibility for Meclofenamate Sodium. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 071468
The FDA assigned number to Meclofenamate Sodium. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Meclofenamate Sodium. 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 - Apr 15, 1987
The date Meclofenamate Sodium 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 Meclofenamate Sodium. 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 Meclofenamate Sodium is in. Format is RX, OTC, DISCN.

Applicant Full Name - Watson Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Meclofenamate Sodium.

Meclofenamate Sodium