Prescription drug · ANDA
Famotidine NDC 70771-1702
Famotidine 20 mg/1 · Tablet, Film coated · Oral · Zydus Lifesciences Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70771-1702-0 | 70771170200 | 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1702-0)Marketed from Jun 6, 2022 | |
| 70771-1702-1 | 70771170201 | 100 TABLET, FILM COATED in 1 BOTTLE (70771-1702-1)Marketed from Jun 6, 2022 | |
| 70771-1702-3 | 70771170203 | 30 TABLET, FILM COATED in 1 BOTTLE (70771-1702-3)Marketed from Jun 6, 2022 | |
| 70771-1702-4 | 70771170204 | 10 BLISTER PACK in 1 CARTON (70771-1702-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1702-2)Marketed from Jun 6, 2022 | |
| 70771-1702-5 | 70771170205 | 500 TABLET, FILM COATED in 1 BOTTLE (70771-1702-5)Marketed from Jun 6, 2022 |
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)
- Famotidine
- Generic name (nonproprietary)
- famotidine
- Active ingredients
- Famotidine — 20 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Zydus Lifesciences Limited
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 216441
- Marketing start
- Listing expires
- Other FDA classes
- Histamine H2 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 70771-1702_33e9f14f-e971-4fbb-9912-991661ae4d05SPL ID 33e9f14f-e971-4fbb-9912-991661ae4d05SPL set ID 8c17f9e3-9827-4bf9-85ca-72e08a8518caRxCUI 284245, 310273UNII 5QZO15J2Z8
- Pharmacologic class
- Histamine-2 Receptor Antagonist
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
N470771170200followed by a unit qualifier and the quantityPackage 70771-1702-00. 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 216441
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 |
|---|---|---|---|---|
| Famotidine | Famotidine 40 mg/1 | Tablet, Film coatedOral | St. Mary's Medical Park Pharmacy | 60760-736 |
| Famotidine | Famotidine 40 mg/1 | Tablet, Film coatedOral | Zydus Lifesciences Limited | 70771-1703 |
| Famotidine | Famotidine 40 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-9615 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-2190 |
| Famotidine | Famotidine 40 mg/1 | Tablet, Film coatedOral | NuCare Pharmaceuticals,Inc. | 68071-3521 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Zydus Pharmaceuticals USA Inc. | 70710-1683 |
| Famotidine | Famotidine 40 mg/1 | Tablet, Film coatedOral | Zydus Pharmaceuticals USA Inc. | 70710-1684 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Safecor Health, LLC | 48433-150 |