Leucovorin Calcium

   
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Leucovorin Calcium


Drug - Leucovorin Calcium
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) - Leucovorin Calcium
Multiple ingredients are in alphabetical order.

Strength - EQ 5MG BASE
The potency of the active ingredient(s), Leucovorin Calcium. May repeat for multiple part products.

Applicant - PAR PHARM
The firm name holding legal responsibility for Leucovorin Calcium. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 071600
The FDA assigned number to Leucovorin Calcium. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Leucovorin Calcium. 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 14, 1987
The date Leucovorin Calcium 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 Leucovorin Calcium. 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 Leucovorin Calcium is in. Format is RX, OTC, DISCN.

Applicant Full Name - Par Pharmaceutical Inc
The full name of the firm holding legal responsibility for the new application of Leucovorin Calcium.

Leucovorin Calcium