Diphenhydramine Hcl Preservative Free

   
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Diphenhydramine Hcl Preservative Free


Drug - Diphenhydramine Hcl Preservative Free
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) - Diphenhydramine Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 50MG/ML
The potency of the active ingredient(s), Diphenhydramine Hydrochloride. May repeat for multiple part products.

Applicant - INTL MEDICATION
The firm name holding legal responsibility for Diphenhydramine Hcl Preservative Free. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 084094
The FDA assigned number to Diphenhydramine Hcl Preservative Free. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Diphenhydramine Hcl Preservative Free. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

Therapeutic Equivalence (TE) Code - AP
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.

Approval Date - Approved Prior to Jan 1, 1982
The date Diphenhydramine Hcl Preservative Free 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 Diphenhydramine Hcl Preservative Free. 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 Diphenhydramine Hcl Preservative Free is in. Format is RX, OTC, DISCN.

Applicant Full Name - International Medication System
The full name of the firm holding legal responsibility for the new application of Diphenhydramine Hcl Preservative Free.

Diphenhydramine Hcl Preservative Free