Over-the-counter drug · ANDA
Zantac 360 (Famotidine) NDC 85237-1926
Famotidine 20 mg/1 · Tablet, Film coated · Oral · Select Consumer Group LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 85237-1926-1 | 8523719260185237192601 | 1 BLISTER PACK in 1 CONTAINER (85237-1926-1) / 1 TABLET, FILM COATED in 1 BLISTER PACK (85237-1926-0)Marketed from Jun 4, 2025 | |
| 85237-1926-2 | 8523719260285237192602 | 2 BLISTER PACK in 1 CONTAINER (85237-1926-2) / 1 TABLET, FILM COATED in 1 BLISTER PACK (85237-1926-0)Marketed from Jun 4, 2025 |
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)
- Zantac 360
- Generic name (nonproprietary)
- famotidine
- Active ingredients
- Famotidine — 20 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Select Consumer Group LLCNDC labeler code 85237
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 206531
- Marketing start
- Listing expires
- Other FDA classes
- Histamine H2 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 85237-1926_554485e1-6776-5eb3-e063-6394a90a7c6bSPL ID 554485e1-6776-5eb3-e063-6394a90a7c6bSPL set ID 529cef2d-e6cc-3b37-e063-6294a90aff59RxCUI 310273, 2609246UNII 5QZO15J2Z8UPC 0655708119266, 0655708219263
- 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
N485237192601followed by a unit qualifier and the quantityPackage 85237-1926-01. 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)
Use s ■ 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.
About NDC 85237-1926
- What is NDC 85237-1926?
- 85237-1926 is the product NDC for Zantac 360 (famotidine), Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Select Consumer Group LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Zantac 360 (Famotidine).
- What is the active ingredient?
- Famotidine.
- Who is the labeler?
- Select Consumer Group LLC, NDC labeler code 85237. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Zantac 360?
- 3 other product NDCs are listed under this name. See all Zantac 360 NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Zantac 360 products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Zantac 360famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Navajo Manufacturing Company Inc. | 67751-214 | 67751-0214-0167751-0214-02 |
| Zantac 360famotidine tablet, film-coated | Famotidine 20 mg/1 | Tablet, Film coatedOral | Lil' Drug Store Products, Inc | 66715-9758 | 66715-9758-0266715-9758-05 |
| Zantac 360famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Chattem, Inc. | 41167-0361 | 41167-0361-0041167-0361-0141167-0361-02+4 more |
Other NDCs under ANDA 206531
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 |
|---|---|---|---|---|
| Amazon Basic Care Acid Reducerfamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Amazon.com Services LLC | 72288-363 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | WALGREEN CO. | 0363-1899 |
| Famotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | WALGREEN CO. | 0363-4400 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | WALGREEN CO. | 0363-5300 |
| Famotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | WALGREEN CO. | 0363-9607 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Better Living Brands, LLC | 21130-033 |
| Famotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | Better Living Brands LLC | 21130-039 |
| Famotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | Amerisource Bergen | 46122-735 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Amerisource Bergen | 46122-737 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Wal-Mart Stores, Inc. | 49035-505 |
| Famotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | Wal-Mart Stores, Inc. | 49035-589 |
| Famotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | Magno-Humphries, Inc. | 54257-180 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Magno-Humphries, Inc. | 54257-802 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Fred's, Inc. | 55315-435 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Family Dollar Stores, LLC | 55319-057 |
| Famotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | Aurohealth LLC | 58602-705 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Aurohealth LLC | 58602-706 |
| Famotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | Aurohealth LLC | 58602-828 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Aurohealth LLC | 58602-829 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Aurohealth LLC | 58602-859 |
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