Hydergine Lc

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Hydergine Lc

Drug - Hydergine Lc
The trade name of the product as shown on the labeling.

The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Ergoloid Mesylates
Multiple ingredients are in alphabetical order.

Strength - 1MG
The potency of the active ingredient(s), Ergoloid Mesylates. May repeat for multiple part products.

Applicant - NOVARTIS
The firm name holding legal responsibility for Hydergine Lc. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 018706
The FDA assigned number to Hydergine Lc. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Hydergine Lc. 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 - Jan 18, 1983
The date Hydergine Lc 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 Hydergine Lc. 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 Hydergine Lc is in. Format is RX, OTC, DISCN.

Applicant Full Name - Novartis Pharmaceuticals Corp
The full name of the firm holding legal responsibility for the new application of Hydergine Lc.

Hydergine Lc