Pentazocine And Naloxone Hydrochlorides

   
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Pentazocine And Naloxone Hydrochlorides


Drug - Pentazocine And Naloxone Hydrochlorides
The trade name of the product as shown on the labeling.

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

Active Ingredient(s) - Naloxone Hydrochloride; Pentazocine Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - EQ 0.5MG BASE;EQ 50MG BASE
The potency of the active ingredient(s), Naloxone Hydrochloride; Pentazocine Hydrochloride. May repeat for multiple part products.

Applicant - RANBAXY
The firm name holding legal responsibility for Pentazocine And Naloxone Hydrochlorides. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 075523
The FDA assigned number to Pentazocine And Naloxone Hydrochlorides. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Pentazocine And Naloxone Hydrochlorides. 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 - Mar 17, 2000
The date Pentazocine And Naloxone Hydrochlorides 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 Pentazocine And Naloxone Hydrochlorides. 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 Pentazocine And Naloxone Hydrochlorides is in. Format is RX, OTC, DISCN.

Applicant Full Name - Ranbaxy Pharmaceuticals Inc
The full name of the firm holding legal responsibility for the new application of Pentazocine And Naloxone Hydrochlorides.

Pentazocine And Naloxone Hydrochlorides