Over-the-counter drug · ANDA
Original strength heartburn prevention NDC 41226-719
famotidine · Famotidine 10 mg/1 · Tablet · Oral · KROGER COMPANY
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 41226-719-06 | 41226071906 | 3 BLISTER PACK in 1 CARTON (41226-719-06) / 10 TABLET in 1 BLISTER PACKMarketed from May 5, 2023 | |
| 41226-719-09 | 41226071909 | 1 BOTTLE in 1 CARTON (41226-719-09) / 90 TABLET in 1 BOTTLEMarketed from Apr 15, 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)
- Original strength heartburn prevention
- Generic name (nonproprietary)
- famotidine
- Active ingredients
- Famotidine — 10 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- KROGER COMPANY
- 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 41226-719_1cb86ee4-41c1-1196-e063-6394a90a9199SPL ID 1cb86ee4-41c1-1196-e063-6394a90a9199SPL set ID ea1c2838-acbd-18e0-e053-2a95a90a3522RxCUI 199047UNII 5QZO15J2Z8UPC 0041260018459
- 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
N441226071906followed by a unit qualifier and the quantityPackage 41226-0719-06. 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 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 |
|---|---|---|---|---|
| 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 |
| Famotidine 20 mg | Famotidine 20 mg/1 | Tablet, CoatedOral | MARKSANS PHARMA LIMITED | 25000-124 |