Prescription drug · ANDA
Famotidine NDC 51655-102
Famotidine 40 mg/1 · Tablet, Film coated · Oral · Northwind Health Company, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 51655-102-26 | 51655010226 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-102-26)Marketed from Jan 25, 2023 | |
| 51655-102-30 | 51655010230 | 30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (51655-102-30)Marketed from Aug 25, 2014 |
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
- Brand name (proprietary)
- Famotidine
- Generic name (nonproprietary)
- famotidine
- Active ingredients
- Famotidine — 40 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 075511
- Marketing start
- Listing expires
- Other FDA classes
- Histamine H2 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 51655-102_46e32413-ef7f-4882-e063-6394a90a78a0SPL ID 46e32413-ef7f-4882-e063-6394a90a78a0SPL set ID 03503cd5-bd8e-4bff-b90d-1a71c5225b91RxCUI 284245UNII 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
N451655010226followed by a unit qualifier and the quantityPackage 51655-0102-26. 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 .
Indications (excerpt from the label)
Famotidine tablets are indicated in adult and pediatric patients 40 kg and greater for the treatment of: active duodenal ulcer (DU). active gastric ulcer (GU). symptomatic nonerosive gastroesophageal reflux disease (GERD). erosive esophagitis due to GERD, diagnosed by biopsy. Famotidine tablets are indicated in adults for the: treatment of pathological hypersecretory conditions (e.g., Zollinger-Ellison syndrome, multiple endocrine neoplasias). reduction of the risk of duodenal ulcer recurrence. Famotidine tablets are a histamine-2 (H 2 ) receptor antagonist indicated (1 ): In adult and pediatric patients 40 kg and greater for the treatment of: active duodenal ulcer (DU). active gastric ulcer…
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 075511
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 20 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 71205-276 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Teva Pharmaceuticals USA, Inc. | 0172-5728 |
| Famotidine | Famotidine 40 mg/1 | Tablet, Film coatedOral | Teva Pharmaceuticals USA, Inc. | 0172-5729 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-1044 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 51655-233 |
| Famotidine | Famotidine 40 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 43063-533 |
| Famotidine | Famotidine 40 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 71205-781 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-6932 |