Prescription drug · ANDA
Pantoprazole NDC 67296-2355
Pantoprazole sodium 40 mg/1 · Tablet, Delayed release · Oral · Redpharm Drug
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 67296-2355-2 | 6729623550267296235502 | 14 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-2355-2)Marketed from Jan 19, 2011 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
- Brand name (proprietary)
- Pantoprazole
- Generic name (nonproprietary)
- pantoprazole
- Active ingredients
- Pantoprazole sodium — 40 mg/1
- Dosage form
- Tablet, Delayed release
- Route
- Oral
- Labeler
- Redpharm DrugNDC labeler code 67296
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 077619
- Marketing start
- Listing expires
- Other FDA classes
- Proton Pump Inhibitors (Mechanism)
- Identifiers
- Product ID 67296-2355_5f1f269d-8ca5-4ae8-e063-6394a90a9de3SPL ID 5f1f269d-8ca5-4ae8-e063-6394a90a9de3
- Pharmacologic class
- Proton Pump Inhibitor
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 HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N467296235502followed by a unit qualifier and the quantityPackage 67296-2355-02. 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.
About NDC 67296-2355
- What is NDC 67296-2355?
- 67296-2355 is the product NDC for Pantoprazole, Pantoprazole sodium 40 mg/1 tablet, delayed release, listed with the FDA by Redpharm Drug. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Pantoprazole.
- What is the active ingredient?
- Pantoprazole sodium.
- Who is the labeler?
- Redpharm Drug, NDC labeler code 67296. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Pantoprazole?
- 11 other product NDCs are listed under this name. See all Pantoprazole NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Pantoprazole products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Pantoprazole | Pantoprazole sodium 20 mg/1 | Tablet, Delayed releaseOral | Coupler LLC | 67046-0789 | 67046-0789-03 |
| Pantoprazole | Pantoprazole sodium 20 mg/1 | Tablet, Delayed releaseOral | Advanced Rx of Tennessee, LLC | 80425-0552 | 80425-0552-0180425-0552-0280425-0552-03 |
| Pantoprazole | Pantoprazole sodium 20 mg/1 | Tablet, Delayed releaseOral | NuCare Pharmaceuticals, Inc. | 68071-3776 | 68071-3776-0368071-3776-06 |
| Pantoprazole | Pantoprazole sodium 40 mg/1 | Tablet, Delayed releaseOral | NuCare Pharmaceuticals,Inc. | 68071-3995 | 68071-3995-09 |
| Pantoprazole | Pantoprazole sodium 20 mg/1 | Tablet, Delayed releaseOral | NorthStar RxLLC | 72603-177 | 72603-0177-01 |
| Pantoprazole | Pantoprazole sodium 40 mg/1 | Tablet, Delayed releaseOral | NorthStar RxLLC | 72603-178 | 72603-0178-01 |
| Pantoprazole | Pantoprazole sodium 20 mg/1 | Tablet, Delayed releaseOral | Preferred Pharmaceuticals Inc. | 68788-8505 | 68788-8505-0168788-8505-0368788-8505-06+2 more |
| Pantoprazole | Pantoprazole sodium 20 mg/1 | Tablet, Delayed releaseOral | St. Mary's Medical Park Pharmacy | 60760-574 | 60760-0574-3060760-0574-60 |
| Pantoprazole | Pantoprazole sodium 20 mg/1 | Tablet, Delayed releaseOral | Dr.Reddy's Laboratories Limited | 55111-332 | 55111-0332-0155111-0332-0555111-0332-10+4 more |
| Pantoprazole | Pantoprazole sodium 40 mg/1 | Tablet, Delayed releaseOral | Dr.Reddy's Laboratories Limited | 55111-333 | 55111-0333-0155111-0333-0555111-0333-10+4 more |
Other NDCs under ANDA 077619
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Pantoprazole | Pantoprazole sodium 20 mg/1 | Tablet, Delayed releaseOral | Coupler LLC | 67046-0789 |
| Pantoprazole | Pantoprazole sodium 20 mg/1 | Tablet, Delayed releaseOral | Dr.Reddy's Laboratories Limited | 55111-332 |
| Pantoprazole | Pantoprazole sodium 40 mg/1 | Tablet, Delayed releaseOral | Dr.Reddy's Laboratories Limited | 55111-333 |
| Pantoprazole | Pantoprazole sodium 40 mg/1 | Tablet, Delayed releaseOral | NuCare Pharmaceuticals,Inc. | 68071-3995 |
| Pantoprazole | Pantoprazole sodium 20 mg/1 | Tablet, Delayed releaseOral | Advanced Rx of Tennessee, LLC | 80425-0552 |
| Pantoprazole | Pantoprazole sodium 40 mg/1 | Tablet, Delayed releaseOral | NuCare Pharmaceuticals,Inc. | 68071-3524 |
| Pantoprazole | Pantoprazole sodium 20 mg/1 | Tablet, Delayed releaseOral | NuCare Pharmaceuticals, Inc. | 68071-3776 |
| Pantoprazole | Pantoprazole sodium 20 mg/1 | Tablet, Delayed releaseOral | St. Mary's Medical Park Pharmacy | 60760-574 |
| Pantoprazole | Pantoprazole sodium 20 mg/1 | Tablet, Delayed releaseOral | Preferred Pharmaceuticals Inc. | 68788-8505 |
| Pantoprazole | Pantoprazole sodium 40 mg/1 | Tablet, Delayed releaseOral | NorthStar RxLLC | 72603-178 |
| Pantoprazole | Pantoprazole sodium 20 mg/1 | Tablet, Delayed releaseOral | NorthStar RxLLC | 72603-177 |
| Pantoprazole | Pantoprazole sodium 20 mg/1 | Tablet, Delayed releaseOral | PHOENIX RX LLC | 85509-1332 |