Hydroxyprogesterone Caproate

   
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Hydroxyprogesterone Caproate


Drug - Hydroxyprogesterone Caproate
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) - Hydroxyprogesterone Caproate
Multiple ingredients are in alphabetical order.

Strength - 250MG/ML
The potency of the active ingredient(s), Hydroxyprogesterone Caproate. May repeat for multiple part products.

Applicant - WATSON LABS
The firm name holding legal responsibility for Hydroxyprogesterone Caproate. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 017439
The FDA assigned number to Hydroxyprogesterone Caproate. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Hydroxyprogesterone Caproate. 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 Hydroxyprogesterone Caproate 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 Hydroxyprogesterone Caproate. 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 Hydroxyprogesterone Caproate is in. Format is RX, OTC, DISCN.

Applicant Full Name - Watson Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Hydroxyprogesterone Caproate.

Hydroxyprogesterone Caproate