Nafcillin Sodium

   
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Nafcillin Sodium


Drug - Nafcillin Sodium
The trade name of the product as shown on the labeling.

Dosage - INJECTABLE; INJECTION
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Nafcillin Sodium
Multiple ingredients are in alphabetical order.

Strength - EQ 4GM BASE/VIAL
The potency of the active ingredient(s), Nafcillin Sodium. May repeat for multiple part products.

Applicant - MARSAM PHARMS LLC
The firm name holding legal responsibility for Nafcillin Sodium. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 062844
The FDA assigned number to Nafcillin Sodium. Format is nnnnnn.

Product Number - 005
The FDA assigned number to identify Nafcillin Sodium. 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 - Oct 26, 1988
The date Nafcillin Sodium 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 Nafcillin Sodium. 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 Nafcillin Sodium is in. Format is RX, OTC, DISCN.

Applicant Full Name - Marsam Pharmaceuticals Llc
The full name of the firm holding legal responsibility for the new application of Nafcillin Sodium.

Nafcillin Sodium