Rifampin And Isoniazid
Drug - Rifampin And Isoniazid
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) -
Isoniazid; Rifampin
Multiple ingredients are in alphabetical order.
Strength -
150MG;300MG
The potency of the active ingredient(s), Isoniazid; Rifampin. May repeat for multiple part products.
Applicant -
WESTWARD
The firm name holding legal responsibility for Rifampin And Isoniazid. The firm name is condensed to a maximum twenty character unique string.
New Drug Application (NDA) Number -
065221
The FDA assigned number to Rifampin And Isoniazid. Format is nnnnnn.
Product Number -
001
The FDA assigned number to identify Rifampin And Isoniazid. 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 -
Jul 29, 2005
The date Rifampin And Isoniazid 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 Rifampin And Isoniazid. 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 Rifampin And Isoniazid is in. Format is RX, OTC, DISCN.
Applicant Full Name -
Westward Pharmaceutical Corp
The full name of the firm holding legal responsibility for the new application of Rifampin And Isoniazid.
Rifampin And Isoniazid
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