Over-the-counter drug · ANDA
Goodmeds Famotidine 20mg 500 count NDC 82725-4047
famotidine 20mg · Famotidine 20 mg/1 · Tablet · Oral · Cabinet Health P.B.C.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 82725-4047-1 | 82725404701 | 500 TABLET in 1 BOTTLE (82725-4047-1)Marketed from Jul 3, 2026 |
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)
- Goodmeds Famotidine 20mg 500 count
- Generic name (nonproprietary)
- famotidine 20mg
- Active ingredients
- Famotidine — 20 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Cabinet Health P.B.C.
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 215766
- Marketing start
- Listing expires
- Other FDA classes
- Histamine H2 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 82725-4047_5592d0f0-03fe-c914-e063-6294a90a2826SPL ID 5592d0f0-03fe-c914-e063-6294a90a2826SPL set ID 5592d0f0-03fd-c914-e063-6294a90a2826RxCUI 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
N482725404701followed by a unit qualifier and the quantityPackage 82725-4047-01. 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)
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 215766
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 10 mg/1 | Tablet, Film coatedOral | CHAIN DRUG MARKETING ASSOCIATION, INC. | 83324-003 |
| famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | CHAIN DRUG MARKETING ASSOCIATION, INC. | 83324-008 |
| Famotidine | Famotidine 10 mg/10mg | TabletOral | Little Pharma, Inc. | 72559-038 |
| famotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | Camber Consumer Care Inc | 69230-326 |
| famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Camber Consumer Care Inc | 69230-327 |
| Heartburn Relieffamotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | Shield Pharmaceuticals Corp | 83059-0031 |