Acetaminophen And Hydrocodone Bitartrate


Acetaminophen And Hydrocodone Bitartrate

Drug - Acetaminophen And Hydrocodone Bitartrate
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) - Acetaminophen; Hydrocodone Bitartrate
Multiple ingredients are in alphabetical order.

Strength - 500MG;5MG
The potency of the active ingredient(s), Acetaminophen; Hydrocodone Bitartrate. May repeat for multiple part products.

Applicant - CENT PHARMS
The firm name holding legal responsibility for Acetaminophen And Hydrocodone Bitartrate. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 088898
The FDA assigned number to Acetaminophen And Hydrocodone Bitartrate. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Acetaminophen And Hydrocodone Bitartrate. 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 - Mar 27, 1985
The date Acetaminophen And Hydrocodone Bitartrate 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 Acetaminophen And Hydrocodone Bitartrate. 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 Acetaminophen And Hydrocodone Bitartrate is in. Format is RX, OTC, DISCN.

Applicant Full Name - Central Pharmaceuticals Inc
The full name of the firm holding legal responsibility for the new application of Acetaminophen And Hydrocodone Bitartrate.

Acetaminophen And Hydrocodone Bitartrate