Acebutolol Hcl

   
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Acebutolol Hcl


Drug - Acebutolol Hcl
The trade name of the product as shown on the labeling.

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

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

Strength - EQ 400MG BASE
The potency of the active ingredient(s), Acebutolol Hydrochloride. May repeat for multiple part products.

Applicant - ALPHAPHARM
The firm name holding legal responsibility for Acebutolol Hcl. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 075047
The FDA assigned number to Acebutolol Hcl. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Acebutolol Hcl. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

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

Approval Date - Dec 30, 1999
The date Acebutolol Hcl 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 Acebutolol Hcl. 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 Acebutolol Hcl is in. Format is RX, OTC, DISCN.

Applicant Full Name - Alphapharm Pty Ltd
The full name of the firm holding legal responsibility for the new application of Acebutolol Hcl.

Acebutolol Hcl