Tagamet Tablet
NDC Package 63029-222-06

The code 63029-222-06 identifies a specific commercial package of 7 blister pack in 1 box / 10 tablet in 1 blister pack of Tagamet, a human over the counter drug labeled by Medtech Products Inc.. This tablet is formulated for oral use and contains cimetidine as the active substance.

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Medtech Products Inc. on June 01, 2012. The current certification is valid through December 31, 2026.

Cimetidine is used to treat ulcers of the stomach and intestines and prevent them from coming back after they have healed. This medication is also used to treat certain stomach and throat (esophagus) problems caused by too much stomach acid (e.g., Zollinger-Ellison syndrome, erosive esophagitis) or a backward flow of stomach acid into the esophagus (acid reflux disease/GERD). Decreasing extra stomach acid can help relieve symptoms such as stomach pain, heartburn, difficulty swallowing, persistent cough, and trouble sleeping. It can also prevent serious acid damage to your digestive system (e.g., ulcers, cancer of the esophagus). Cimetidine belongs to a class of drugs commonly called H2 blockers. It works by reducing the amount of acid in your stomach. This medication is also available without a prescription. It is used to treat occasional heartburn caused by too much acid in the stomach (also called acid indigestion or sour stomach). It is also used to prevent heartburn and acid indigestion caused by certain foods and beverages. If you are taking this medication for self-treatment, it is important to read the manufacturer's package instructions carefully so you know when to consult your doctor or pharmacist. (See also Precautions.)

For medical billing and reimbursement, this package follows the 11-digit CMS format: 63029022206. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.