Hydrocortisone In Absorbase

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Hydrocortisone In Absorbase

Drug - Hydrocortisone In Absorbase
The trade name of the product as shown on the labeling.

The product dosage form and route separated by a semi-colon.

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

Strength - 1%
The potency of the active ingredient(s), Hydrocortisone. May repeat for multiple part products.

The firm name holding legal responsibility for Hydrocortisone In Absorbase. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 088138
The FDA assigned number to Hydrocortisone In Absorbase. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Hydrocortisone In Absorbase. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

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

Approval Date - Sep 6, 1985
The date Hydrocortisone In Absorbase 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 Hydrocortisone In Absorbase. 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 Hydrocortisone In Absorbase is in. Format is RX, OTC, DISCN.

Applicant Full Name - Carolina Medical Products Co
The full name of the firm holding legal responsibility for the new application of Hydrocortisone In Absorbase.

Hydrocortisone In Absorbase