Ortho-novum 7/7/7-21

   
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Ortho-novum 7/7/7-21


Drug - Ortho-novum 7/7/7-21
The trade name of the product as shown on the labeling.

Dosage - TABLET; ORAL-21
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Ethinyl Estradiol; Norethindrone
Multiple ingredients are in alphabetical order.

Strength - 0.035MG,0.035MG,0.035MG;0.5MG,0.75MG,1MG
The potency of the active ingredient(s), Ethinyl Estradiol; Norethindrone. May repeat for multiple part products.

Applicant - ORTHO MCNEIL PHARM
The firm name holding legal responsibility for Ortho-novum 7/7/7-21. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 018985
The FDA assigned number to Ortho-novum 7/7/7-21. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Ortho-novum 7/7/7-21. 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 - Apr 4, 1984
The date Ortho-novum 7/7/7-21 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 Ortho-novum 7/7/7-21. 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 Ortho-novum 7/7/7-21 is in. Format is RX, OTC, DISCN.

Applicant Full Name - Ortho Mcneil Pharmaceutical Inc
The full name of the firm holding legal responsibility for the new application of Ortho-novum 7/7/7-21.

Ortho-novum 7/7/7-21