Over-the-counter drug · ANDA
Heartburn Relief (Famotidine) NDC 83059-0005
Famotidine 10 mg/1 · Tablet, Film coated · Oral · Shield Pharmaceuticals Corp
NDC codes
FDA NDC DirectoryProduct NDC (as listed)83059-0005Labeler and product segments. Claims need a package NDC.
Product NDC at billing width83059-0005Add the package segment from the table below.
| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 83059-0005-5 | 8305900050583059000505 | 1 BOTTLE in 1 PACKAGE (83059-0005-5) / 50 TABLET, FILM COATED in 1 BOTTLEMarketed from Jan 16, 2024 |
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)
- Heartburn Relief
- Generic name (nonproprietary)
- famotidine
- Active ingredients
- Famotidine — 10 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Shield Pharmaceuticals CorpNDC labeler code 83059
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 215822
- Marketing start
- Listing expires
- Other FDA classes
- Histamine H2 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 83059-0005_5c3f8f38-4409-6c3b-e063-6294a90a22dcSPL ID 5c3f8f38-4409-6c3b-e063-6294a90a22dc
- 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
N483059000505followed by a unit qualifier and the quantityPackage 83059-0005-05. 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
The FDA listing for this product does not reference a label (SPL) set.
About NDC 83059-0005
- What is NDC 83059-0005?
- 83059-0005 is the product NDC for Heartburn Relief (famotidine), Famotidine 10 mg/1 tablet, film coated, listed with the FDA by Shield Pharmaceuticals Corp. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Heartburn Relief (Famotidine).
- What is the active ingredient?
- Famotidine.
- Who is the labeler?
- Shield Pharmaceuticals Corp, NDC labeler code 83059. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Heartburn Relief?
- 8 other product NDCs are listed under this name. See all Heartburn Relief NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Heartburn 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) |
|---|---|---|---|---|---|
| Heartburn Relieffamotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | Shield Pharmaceuticals Corp | 83059-0185 | 83059-0185-01 |
| Heartburn Reliefaluminum hydroxide and magnesium carbonate | Aluminum hydroxide 254 mg/5mL; Magnesium carbonate 237.5 mg/5mL | SuspensionOral | GERI-CARE PHARMACEUTICALS, CORP | 57896-565 | 57896-0565-12 |
| Heartburn Relieffamotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | Shield Pharmaceuticals Corp | 83059-0031 | 83059-0031-05 |
| Heartburn Reliefaluminum hydroxide and magnesium carbonate | Aluminum hydroxide 254 mg/5mL; Magnesium carbonate 237.5 mg/5mL | SuspensionOral | CHAIN DRUG MARKETING ASSOCIATION | 63868-565 | 63868-0565-12 |
| heartburn relieffamotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | Meijer Distribution Inc | 41250-493 | 41250-0493-6541250-0493-72 |
| heartburn relieffamotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Meijer Distribution Inc | 41250-712 | 41250-0712-0241250-0712-7141250-0712-78 |
| Heartburn Reliefcarbo more | Activated charcoal 6 [hp_X]/1 + 5 more ingredients | Tablet, Orally disintegratingOral | TRP Company | 17312-030 | 17312-0030-14 |
| heartburn reliefcimetidine | Cimetidine 200 mg/1 | Tablet, Film coatedOral | CVS Pharmacy | 59779-022 | 59779-0022-7259779-0022-76 |
Other NDCs under ANDA 215822
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 | VKT Pharma Private Limited | 71821-012 |
| Famotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | VKT Pharma Private Limited | 71821-012 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | TWIN MED LLC | 55681-342 |
| Famotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | TWIN MED LLC | 55681-343 |
| Curist Acid Relieffamotidine 20 mg | Famotidine 20 mg/1 | TabletOral | Little Pharma, Inc. | 72559-032 |
| Heartburn Relieffamotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | Shield Pharmaceuticals Corp | 83059-0185 |
| Famotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | GLENMARK THERAPEUTICS INC., USA | 72657-112 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | GLENMARK THERAPEUTICS INC., USA | 72657-113 |
| Famotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | FAMILY DOLLAR | 55319-408 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | FAMILY DOLLAR | 55319-409 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | GLENMARK THERAPEUTICS INC., USA | 72657-132 |
| Famotidine | Famotidine 10 mg/1 | TabletOral | Bi-Mart | 37835-161 |
| Famotidine | Famotidine 20 mg/1 | TabletOral | Bi-Mart | 37835-165 |
| Famotidine | Famotidine 10 mg/1 | Tablet, Film coatedOral | GERI-CARE PHARMACEUTICAL CORP | 57896-317 |
| Famotidine | Famotidine 20 mg/1 | Tablet, Film coatedOral | Geri-Care Pharmaceutical Corp | 57896-319 |
| Acid Reducer Maximum Strengthfamotidine 20mg | Famotidine 20 mg/1 | TabletOral | Grocery Outlet | 85828-443 |
| Welmate Famotidine 20mgfamotidine 20mg | Famotidine 20 mg/1 | TabletOral | YYBA Corp | 73581-109 |
| Welmate Famotidine 10mgfamotidine 10mg | Famotidine 10 mg/1 | TabletOral | YYBA Corp | 73581-108 |
| Famotidine | Famotidine 20 mg/1 | TabletOral | SAFEWAY | 21130-191 |
| Acid Reducer | Famotidine 20 mg/1 | TabletOral | Demoulas Super Markets, Inc. | 53942-443 |
Showing 20 of 23.