Acetaminophen And Pentazocine Hcl
Drug - Acetaminophen And Pentazocine Hcl
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) -
Acetaminophen; Pentazocine Hydrochloride
Multiple ingredients are in alphabetical order.
Strength -
650MG;EQ 25MG BASE
The potency of the active ingredient(s), Acetaminophen; Pentazocine Hydrochloride. May repeat for multiple part products.
Applicant -
AMIDE PHARM
The firm name holding legal responsibility for Acetaminophen And Pentazocine Hcl. The firm name is condensed to a maximum twenty character unique string.
New Drug Application (NDA) Number -
076202
The FDA assigned number to Acetaminophen And Pentazocine Hcl. Format is nnnnnn.
Product Number -
001
The FDA assigned number to identify Acetaminophen And Pentazocine 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 -
Aug 2, 2002
The date Acetaminophen And Pentazocine 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 Acetaminophen And Pentazocine 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 Acetaminophen And Pentazocine Hcl is in. Format is RX, OTC, DISCN.
Applicant Full Name -
Amide Pharmaceutical Inc
The full name of the firm holding legal responsibility for the new application of Acetaminophen And Pentazocine Hcl.
Acetaminophen And Pentazocine Hcl
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