Aventyl Hcl
Drug - Aventyl Hcl
The trade name of the product as shown on the labeling.
Dosage -
CAPSULE; ORAL
The product dosage form and route separated by a semi-colon.
Active Ingredient(s) -
Nortriptyline Hydrochloride
Multiple ingredients are in alphabetical order.
Strength -
EQ 25MG BASE
The potency of the active ingredient(s), Nortriptyline Hydrochloride. May repeat for multiple part products.
Applicant -
LILLY
The firm name holding legal responsibility for Aventyl Hcl. The firm name is condensed to a maximum twenty character unique string.
New Drug Application (NDA) Number -
014684
The FDA assigned number to Aventyl Hcl. Format is nnnnnn.
Product Number -
002
The FDA assigned number to identify Aventyl Hcl. 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 -
Approved Prior to Jan 1, 1982
The date Aventyl Hcl 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 Aventyl Hcl. 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 Aventyl Hcl is in. Format is RX, OTC, DISCN.
Applicant Full Name -
Eli Lilly And Co
The full name of the firm holding legal responsibility for the new application of Aventyl Hcl.
Aventyl Hcl
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