Bulk ingredient · DRUG FOR FURTHER PROCESSING
Pantoprazole NDC 55111-333
Pantoprazole sodium 40 mg/1 · Tablet, Delayed release · Dr. Reddy's Laboratories Limited
Unfinished product
This listing is a bulk ingredient, not a finished drug product dispensed or administered to patients. It is not normally billed.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 55111-333-96 | 55111033396 | 7500 TABLET, DELAYED RELEASE in 1 POUCH (55111-333-96)Marketed from 06-SEP-12 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Generic name (nonproprietary)
- pantoprazole
- Active ingredients
- Pantoprazole sodium — 40 mg/1
- Dosage form
- Tablet, Delayed release
- Product type
- Bulk ingredient
- Marketing category
- Drug for further processing
- Marketing start
- Listing expires
- Identifiers
- Product ID 55111-333_eb5d5907-ad31-800b-5581-fbc20316eabeSPL ID eb5d5907-ad31-800b-5581-fbc20316eabe
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.
- NDC on a medical claim
N455111033396followed by a unit qualifier and the quantityPackage 55111-0333-96. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
The FDA listing for this product does not reference a label (SPL) set.