Nitrolingual Pumpspray

   
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Nitrolingual Pumpspray


Drug - Nitrolingual Pumpspray
The trade name of the product as shown on the labeling.

Dosage - SPRAY, METERED; SUBLINGUAL
The product dosage form and route separated by a semi-colon.

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

Strength - 0.4MG/SPRAY
The potency of the active ingredient(s), Nitroglycerin. May repeat for multiple part products.

Applicant - POHL BOSKAMP
The firm name holding legal responsibility for Nitrolingual Pumpspray. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 018705
The FDA assigned number to Nitrolingual Pumpspray. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Nitrolingual Pumpspray. 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 - Jan 10, 1997
The date Nitrolingual Pumpspray 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 Nitrolingual Pumpspray. 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 Nitrolingual Pumpspray is in. Format is RX, OTC, DISCN.

Applicant Full Name - G Pohl Boskamp Gmbh And Co
The full name of the firm holding legal responsibility for the new application of Nitrolingual Pumpspray.

Nitrolingual Pumpspray