What is NDC 21130-027?

21130-027 is the product NDC for Maximum Strength Acid Controller (famotidine), Famotidine 20 mg/1 tablet, listed with the FDA by BETTER LIVING BRANDS LLC.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Maximum Strength Acid Controller (Famotidine).

BETTER LIVING BRANDS LLC., NDC labeler code 21130. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Maximum Strength Acid Controller?

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.

Maximum Strength Acid Controller NDC 21130-027

NDC codes

FDA NDC Directory

Product NDC (as listed)21130-027Labeler and product segments. Claims need a package NDC.

Product NDC at billing width21130-0027Add 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
21130-027-05	2113000270521130002705	1 BOTTLE in 1 CARTON (21130-027-05) / 50 TABLET in 1 BOTTLEMarketed from Jun 23, 2023

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): Maximum Strength Acid Controller
Generic name (nonproprietary): famotidine
Active ingredients: Famotidine — 20 mg/1
Dosage form: Tablet
Route: Oral
Labeler: BETTER LIVING BRANDS LLC.NDC labeler code 21130
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217543
Marketing start: Jun 23, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 21130-027_01af6236-f4ba-5999-e063-6394a90a3806SPL ID 01af6236-f4ba-5999-e063-6394a90a3806SPL set ID f2c031b4-de86-3a8e-e053-2a95a90a21e0RxCUI 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

N421130002705 followed by a unit qualifier and the quantity

Package 21130-0027-05. 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

Current FDA label (SPL), effective Jul 30, 2023.

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 21130-027

What is NDC 21130-027?: 21130-027 is the product NDC for Maximum Strength Acid Controller (famotidine), Famotidine 20 mg/1 tablet, listed with the FDA by BETTER LIVING BRANDS LLC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Maximum Strength Acid Controller (Famotidine).
What is the active ingredient?: Famotidine.
Who is the labeler?: BETTER LIVING BRANDS LLC., NDC labeler code 21130. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Maximum Strength Acid Controller?: 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 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	25000-087
Famotidine 20 mg	Famotidine 20 mg/1	Tablet, CoatedOral	MARKSANS PHARMA LIMITED	25000-124
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

Maximum Strength Acid Controller (Famotidine) NDC 21130-027