Over-the-counter drug · ANDA
famotidine NDC 83324-008
Famotidine 20 mg/1 · Tablet, Film coated · Oral · CHAIN DRUG MARKETING ASSOCIATION, INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 83324-008-50 | 83324000850 | 1 CONTAINER in 1 CARTON (83324-008-50) / 50 TABLET, FILM COATED in 1 CONTAINERMarketed from Mar 6, 2024 |
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 — 20 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- 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 83324-008_14a35301-b682-06ca-e063-6394a90a7bc6SPL ID 14a35301-b682-06ca-e063-6394a90a7bc6SPL set ID 6daf1ebe-b0a2-4413-bf25-3de6eb64b0c6RxCUI 199047, 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
N483324000850followed by a unit qualifier and the quantityPackage 83324-0008-50. 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)
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 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 |
|---|---|---|---|---|
| Goodmeds Famotidine 20mg 500 countfamotidine 20mg | Famotidine 20 mg/1 | TabletOral | Cabinet Health P.B.C. | 82725-4047 |
| famotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | CHAIN DRUG MARKETING ASSOCIATION, INC. | 83324-003 |
| 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 |