Cold Capsule Iv

   
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Cold Capsule Iv


Drug - Cold Capsule Iv
The trade name of the product as shown on the labeling.

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

Active Ingredient(s) - Chlorpheniramine Maleate; Phenylpropanolamine Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 12MG;75MG
The potency of the active ingredient(s), Chlorpheniramine Maleate; Phenylpropanolamine Hydrochloride. May repeat for multiple part products.

Applicant - GRAHAM DM
The firm name holding legal responsibility for Cold Capsule Iv. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 018793
The FDA assigned number to Cold Capsule Iv. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Cold Capsule Iv. 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 25, 1985
The date Cold Capsule Iv 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 Cold Capsule Iv. 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 Cold Capsule Iv is in. Format is RX, OTC, DISCN.

Applicant Full Name - Dm Graham Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Cold Capsule Iv.

Cold Capsule Iv