Over-the-counter drug · ANDA
Famotidine 20 mg NDC 25000-124
Famotidine 20 mg/1 · Tablet, Coated · Oral · MARKSANS PHARMA LIMITED
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 25000-124-68 | 25000012468 | 300 TABLET, COATED in 1 BOTTLE (25000-124-68)Marketed from May 23, 2025 | |
| 25000-124-84 | 25000012484 | 1 BOTTLE in 1 CARTON (25000-124-84) / 25 TABLET, COATED in 1 BOTTLEMarketed from May 23, 2025 | |
| 25000-124-94 | 25000012494 | 5 BLISTER PACK in 1 CARTON (25000-124-94) / 5 TABLET, COATED in 1 BLISTER PACKMarketed from May 23, 2025 |
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 20 mg
- Generic name (nonproprietary)
- famotidine 20 mg
- Active ingredients
- Famotidine — 20 mg/1
- Dosage form
- Tablet, Coated
- Route
- Oral
- Labeler
- MARKSANS PHARMA LIMITED
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 217543
- Marketing start
- Listing expires
- Other FDA classes
- Histamine H2 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 25000-124_1c69fac1-3052-45b1-ab46-a3b523347de1SPL ID 1c69fac1-3052-45b1-ab46-a3b523347de1SPL set ID 5a66206b-35b1-4d86-8574-a1e45cb0772fRxCUI 310273UNII 5QZO15J2Z8UPC 0325000124847, 0325000124687, 0325000124946
- 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
N425000012468followed by a unit qualifier and the quantityPackage 25000-0124-68. 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)
USE(S) Uses •relieves heartburn associated with acid indigestion and sour stomach •prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain food and beverages
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 217543
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 |
|---|---|---|---|---|
| Original strength heartburn preventionfamotidine | Famotidine 10 mg/1 | TabletOral | KROGER COMPANY | 41226-719 |
| Maximum Strength Acid Reducerfamotidine | Famotidine 20 mg/1 | TabletOral | TARGET CORPORATION | 11673-697 |
| Maximum Strength Acid Reducerfamotidine | Famotidine 20 mg/1 | TabletOral | TIME CAP LABORATORIES,INC | 49483-720 |
| Maximum Strength Acid Controllerfamotidine | Famotidine 20 mg/1 | TabletOral | BETTER LIVING BRANDS LLC. | 21130-027 |
| Famotidine 10 mg | Famotidine 10 mg/1 | Tablet, CoatedOral | MARKSANS PHARMA LIMITED | 25000-086 |
| Famotidine 20 mg | Famotidine 20 mg/1 | Tablet, CoatedOral | MARKSANS PHARMA LIMITED | 25000-087 |