Meperidine Hcl Preservative Free

   
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Meperidine Hcl Preservative Free


Drug - Meperidine Hcl Preservative Free
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) - Meperidine Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 10MG/ML
The potency of the active ingredient(s), Meperidine Hydrochloride. May repeat for multiple part products.

Applicant - MAYNE PHARMA USA
The firm name holding legal responsibility for Meperidine Hcl Preservative Free. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 040305
The FDA assigned number to Meperidine Hcl Preservative Free. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Meperidine Hcl Preservative Free. 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 - Mar 10, 1999
The date Meperidine Hcl Preservative Free 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 Meperidine Hcl Preservative Free. 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 Meperidine Hcl Preservative Free is in. Format is RX, OTC, DISCN.

Applicant Full Name - Mayne Pharma Usa Inc
The full name of the firm holding legal responsibility for the new application of Meperidine Hcl Preservative Free.

Meperidine Hcl Preservative Free