Prescription drug · ANDA
Ibuprofen and Famotidine NDC 70771-1924
Ibuprofen 800 mg/1; Famotidine 26.6 mg/1 · Tablet · Oral · Zydus Lifesciences Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70771-1924-9 | 70771192409 | 90 TABLET in 1 BOTTLE (70771-1924-9)Marketed from Jun 1, 2025 |
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)
- Ibuprofen and Famotidine
- Generic name (nonproprietary)
- ibuprofen and famotidine
- Active ingredients
- Ibuprofen — 800 mg/1Famotidine — 26.6 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Zydus Lifesciences Limited
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 218684
- Marketing start
- Listing expires
- Other FDA classes
- Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Histamine H2 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 70771-1924_099f42a7-f7c9-49f0-8b83-74670cc8124aSPL ID 099f42a7-f7c9-49f0-8b83-74670cc8124aSPL set ID 24204938-0989-42ad-8ad8-89979e62d700RxCUI 1100066UNII WK2XYI10QM, 5QZO15J2Z8
- Pharmacologic class
- Histamine-2 Receptor Antagonist; Nonsteroidal Anti-inflammatory Drug
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
N470771192409followed by a unit qualifier and the quantityPackage 70771-1924-09. 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
Current FDA label (SPL), effective .
Other NDCs under ANDA 218684
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 |
|---|---|---|---|---|
| Ibuprofen Famotidine | Ibuprofen 800 mg/1; Famotidine 26.6 mg/1 | TabletOral | Direct_Rx | 72189-667 |
| Ibuprofen and Famotidine | Ibuprofen 800 mg/1; Famotidine 26.6 mg/1 | TabletOral | Viona Pharmaceuticals Inc | 72578-214 |
| Ibuprofen and Famotidine | Ibuprofen 800 mg/1; Famotidine 26.6 mg/1 | TabletOral | Advanced Rx of Tennessee, LLC | 80425-0587 |