What is NDC 73581-108?

73581-108 is the product NDC for Welmate Famotidine 10mg (famotidine 10mg), Famotidine 10 mg/1 tablet, listed with the FDA by YYBA Corp. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Welmate Famotidine 10mg (Famotidine 10mg).

YYBA Corp, NDC labeler code 73581. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Welmate Famotidine 10mg?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Welmate Famotidine 10mg NDC 73581-108

NDC codes

FDA NDC Directory

Product NDC (as listed)73581-108Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73581-0108Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
73581-108-09	7358101080973581010809	90 TABLET in 1 BOTTLE (73581-108-09)Marketed from Jun 1, 2025
73581-108-10	7358101081073581010810	300 TABLET in 1 BOTTLE (73581-108-10)Marketed from Jul 25, 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): Welmate Famotidine 10mg
Generic name (nonproprietary): famotidine 10mg
Active ingredients: Famotidine — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: YYBA CorpNDC labeler code 73581
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 215822
Marketing start: Jul 25, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 73581-108_3b0b7c5c-9d4e-5cc4-e063-6294a90acecfSPL ID 3b0b7c5c-9d4e-5cc4-e063-6294a90acecfSPL set ID 1e19d0cc-65d7-8ec4-e063-6394a90a3d2aRxCUI 199047UNII 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

N473581010809 followed by a unit qualifier and the quantity

Package 73581-0108-09. 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 Jul 29, 2025.

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.

Full label on DailyMed (opens in a new tab)

About NDC 73581-108

What is NDC 73581-108?: 73581-108 is the product NDC for Welmate Famotidine 10mg (famotidine 10mg), Famotidine 10 mg/1 tablet, listed with the FDA by YYBA Corp. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Welmate Famotidine 10mg (Famotidine 10mg).
What is the active ingredient?: Famotidine.
Who is the labeler?: YYBA Corp, NDC labeler code 73581. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Welmate Famotidine 10mg?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under ANDA 215822

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 215822
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
Heartburn Relieffamotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Shield Pharmaceuticals Corp	83059-0005
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
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.

Welmate Famotidine 10mg (Famotidine 10mg) NDC 73581-108