Loratadine
NDC Package 68071-3203-9

The code 68071-3203-9 identifies a specific commercial package of 90 tablet in 1 bottle of Loratadine, labeled by Nucare Pharmaceuticals, Inc.. This is formulated for use and contains as the active substance.

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Nucare Pharmaceuticals, Inc. on January 21, 2003. The current certification is valid through January 31, 2020.

This medication is an antihistamine that treats symptoms such as itching, runny nose, watery eyes, and sneezing from "hay fever" and other allergies. It is also used to relieve itching from hives. Loratadine does not prevent hives or prevent/treat a serious allergic reaction (anaphylaxis). Therefore, if your doctor has prescribed epinephrine to treat allergic reactions, always carry your epinephrine injector with you. Do not use loratadine in place of your epinephrine. If you are self-treating with this medication, it is important to read the manufacturer's package instructions carefully so you know when to consult your doctor or pharmacist. (See also Precautions section.) If you are using the tablets or capsules, do not use in children younger than 6 years unless directed by the doctor. If you are using the liquid or chewable tablets, do not use in children younger than 2 years unless directed by the doctor.

For medical billing and reimbursement, this package follows the 11-digit CMS format: 68071320309. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.