Phenergan Vc

   
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Phenergan Vc


Drug - Phenergan Vc
The trade name of the product as shown on the labeling.

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

Active Ingredient(s) - Phenylephrine Hydrochloride; Promethazine Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 5MG/5ML;6.25MG/5ML
The potency of the active ingredient(s), Phenylephrine Hydrochloride; Promethazine Hydrochloride. May repeat for multiple part products.

Applicant - WYETH AYERST
The firm name holding legal responsibility for Phenergan Vc. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 008604
The FDA assigned number to Phenergan Vc. Format is nnnnnn.

Product Number - 003
The FDA assigned number to identify Phenergan Vc. 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 - Apr 2, 1984
The date Phenergan Vc 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 Phenergan Vc. 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 Phenergan Vc is in. Format is RX, OTC, DISCN.

Applicant Full Name - Wyeth Ayerst Laboratories
The full name of the firm holding legal responsibility for the new application of Phenergan Vc.

Phenergan Vc