Pharmaseal Scrub Care
Drug - Pharmaseal Scrub Care
The trade name of the product as shown on the labeling.
Dosage -
SPONGE; TOPICAL
The product dosage form and route separated by a semi-colon.
Active Ingredient(s) -
Chlorhexidine Gluconate
Multiple ingredients are in alphabetical order.
Strength -
4%
The potency of the active ingredient(s), Chlorhexidine Gluconate. May repeat for multiple part products.
Applicant -
PHARMASEAL
The firm name holding legal responsibility for Pharmaseal Scrub Care. The firm name is condensed to a maximum twenty character unique string.
New Drug Application (NDA) Number -
019793
The FDA assigned number to Pharmaseal Scrub Care. Format is nnnnnn.
Product Number -
001
The FDA assigned number to identify Pharmaseal Scrub Care. 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 -
Dec 2, 1988
The date Pharmaseal Scrub Care 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 Pharmaseal Scrub Care. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.
Type -
OTC
The group or category of approved drugs Pharmaseal Scrub Care is in. Format is RX, OTC, DISCN.
Applicant Full Name -
Pharmaseal Div Baxter Healthcare Corp
The full name of the firm holding legal responsibility for the new application of Pharmaseal Scrub Care.
Pharmaseal Scrub Care
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