Over-the-counter drug · ANDA
acid relief (Famotidine) NDC 11822-6123
Famotidine 20 mg/1 · Tablet, Film coated · Oral · Rite Aid Corporation
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 11822-6123-0 | 11822612300 | 1 BOTTLE in 1 CARTON (11822-6123-0) / 50 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 19, 2023 |
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)
- acid relief
- Generic name (nonproprietary)
- famotidine
- Active ingredients
- Famotidine — 20 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Rite Aid CorporationNDC labeler code 11822
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 077351
- Marketing start
- Marketing end
- Other FDA classes
- Histamine H2 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 11822-6123_36acfd2a-4d54-46f2-bd9d-4b30eaa2cabeSPL ID 36acfd2a-4d54-46f2-bd9d-4b30eaa2cabeSPL set ID 8c6d5419-088b-4b3e-80b8-2a0d06926ff1RxCUI 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
N411822612300followed by a unit qualifier and the quantityPackage 11822-6123-00. 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.
About NDC 11822-6123
- What is NDC 11822-6123?
- 11822-6123 is the product NDC for acid relief (famotidine), Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Rite Aid Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- acid relief (Famotidine).
- What is the active ingredient?
- Famotidine.
- Who is the labeler?
- Rite Aid Corporation, NDC labeler code 11822. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for acid relief?
- 1 other product NDC are listed under this name. See all acid relief NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other acid relief products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| acid relieffamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Rite Aid Corporation | 11822-1194 | 11822-1194-0111822-1194-0211822-1194-04+1 more |
Other NDCs under ANDA 077351
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 |
|---|---|---|---|---|
| Acid Controllerfamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Walgreen Company | 0363-0701 |
| acid controllerfamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Walgreen Company | 0363-1203 |
| acid controllerfamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Safeway | 21130-521 |
| Acid Controllerfamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | H E B | 37808-042 |
| Acid Controllerfamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | H E B | 59640-001 |
| acid controllerfamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | CVS Pharmacy | 59779-194 |
| Acid Reducerfamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | HyVee Inc | 42507-194 |
| Acid Reducerfamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 51316-511 |
| Acid Reducerfamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Publix Super Markets Inc | 56062-088 |
| acid reducerfamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | H E B | 59640-023 |
| acid reducerfamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | CVS Pharmacy | 69842-659 |
| acid relieffamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Rite Aid Corporation | 11822-1194 |
| basic care acid reducerfamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Amazon.com Services LLC | 72288-194 |
| basic care acid reducerfamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Amazon.com Services LLC | 72288-329 |
| basic care heartburn preventionfamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Amazon.com Services LLC | 72288-151 |
| berkley and jensen famotidinefamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | BJWC | 68391-300 |
| CareOne Acid Relieffamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | American Sales Company | 41520-707 |
| careone acid relieffamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Retail Business Services, LLC | 72476-150 |
| careone acid relieffamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Retail Business Services, LLC | 72476-299 |
| dg health acid reducerfamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Dolgencorp Inc | 55910-814 |
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