Atropine And Demerol

   
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Atropine And Demerol


Drug - Atropine And Demerol
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) - Atropine Sulfate; Meperidine Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 0.4MG/ML;100MG/ML
The potency of the active ingredient(s), Atropine Sulfate; Meperidine Hydrochloride. May repeat for multiple part products.

Applicant - ABBOTT
The firm name holding legal responsibility for Atropine And Demerol. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 087848
The FDA assigned number to Atropine And Demerol. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Atropine And Demerol. 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 - Nov 26, 1982
The date Atropine And Demerol 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 Atropine And Demerol. 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 Atropine And Demerol is in. Format is RX, OTC, DISCN.

Applicant Full Name - Abbott Laboratories
The full name of the firm holding legal responsibility for the new application of Atropine And Demerol.

Atropine And Demerol