What is NDC 25000-087?

25000-087 is the product NDC for Famotidine 20 mg, Famotidine 20 mg/1 tablet, coated, listed with the FDA by MARKSANS PHARMA LIMITED. It has 5 package NDCs, shown above in 10- and 11-digit form.

MARKSANS PHARMA LIMITED, NDC labeler code 25000. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Famotidine 20 mg?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Famotidine 20 mg NDC 25000-087 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)25000-087Labeler and product segments. Claims need a package NDC.

Product NDC at billing width25000-0087Add 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
25000-087-03	2500000870325000008703	1 BOTTLE in 1 CARTON (25000-087-03) / 30 TABLET, COATED in 1 BOTTLEMarketed from Mar 10, 2023
25000-087-05	2500000870525000008705	1 BOTTLE in 1 CARTON (25000-087-05) / 50 TABLET, COATED in 1 BOTTLEMarketed from Apr 24, 2024
25000-087-08	2500000870825000008708	1 BOTTLE in 1 CARTON (25000-087-08) / 100 TABLET, COATED in 1 BOTTLEMarketed from Mar 10, 2023
25000-087-36	2500000873625000008736	3 BLISTER PACK in 1 CARTON (25000-087-36) / 10 TABLET, COATED in 1 BLISTER PACKMarketed from Mar 10, 2023
25000-087-82	2500000878225000008782	1 BOTTLE in 1 CARTON (25000-087-82) / 200 TABLET, COATED in 1 BOTTLEMarketed from Feb 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): Famotidine 20 mg
Generic name (nonproprietary): famotidine 20 mg
Active ingredients: Famotidine — 20 mg/1
Dosage form: Tablet, Coated
Route: Oral
Labeler: MARKSANS PHARMA LIMITEDNDC labeler code 25000
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217543
Marketing start: Mar 10, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 25000-087_c1fe0ae2-1d7b-409d-97cb-9e03eeb7f402SPL ID c1fe0ae2-1d7b-409d-97cb-9e03eeb7f402SPL set ID 58b653eb-6539-4b79-9d22-df6eaf35307fRxCUI 199047, 310273UNII 5QZO15J2Z8UPC 0325000086039, 0325000087364, 0325000086367, 0325000086084, 0325000087081, 0325000087036, 0325000087821
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

N425000008703 followed by a unit qualifier and the quantity

Package 25000-0087-03. 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 Sep 30, 2024.

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 25000-087

What is NDC 25000-087?: 25000-087 is the product NDC for Famotidine 20 mg, Famotidine 20 mg/1 tablet, coated, listed with the FDA by MARKSANS PHARMA LIMITED. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Famotidine 20 mg.
What is the active ingredient?: Famotidine.
Who is the labeler?: MARKSANS PHARMA LIMITED, NDC labeler code 25000. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Famotidine 20 mg?: 1 other product NDC are listed under this name. See all Famotidine 20 mg NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Famotidine 20 mg NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Famotidine 20 mg	Famotidine 20 mg/1	Tablet, CoatedOral	MARKSANS PHARMA LIMITED	25000-124	25000-0124-6825000-0124-8425000-0124-94

Other NDCs under ANDA 217543

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

FDA NDC Directory listings under ANDA 217543
Product	Strength	Form · route	Labeler	Product NDC
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	25000-124
Maximum Strength Acid Controllerfamotidine	Famotidine 20 mg/1	TabletOral	BETTER LIVING BRANDS LLC.	21130-027
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
Original strength heartburn preventionfamotidine	Famotidine 10 mg/1	TabletOral	KROGER COMPANY	41226-719