What is NDC 83324-008?

83324-008 is the product NDC for famotidine, Famotidine 20 mg/1 tablet, film coated, listed with the FDA by CHAIN DRUG MARKETING ASSOCIATION, INC.. It has 1 package NDC, shown above in 10- and 11-digit form.

CHAIN DRUG MARKETING ASSOCIATION, INC., NDC labeler code 83324. 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?

252 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

famotidine NDC 83324-008 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)83324-008Labeler and product segments. Claims need a package NDC.

Product NDC at billing width83324-0008Add 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
83324-008-50	8332400085083324000850	1 CONTAINER in 1 CARTON (83324-008-50) / 50 TABLET, FILM COATED in 1 CONTAINERMarketed from Mar 6, 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
Generic name (nonproprietary): famotidine
Active ingredients: Famotidine — 20 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: CHAIN DRUG MARKETING ASSOCIATION, INC.NDC labeler code 83324
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 215766
Marketing start: Mar 6, 2024
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 83324-008_14a35301-b682-06ca-e063-6394a90a7bc6SPL ID 14a35301-b682-06ca-e063-6394a90a7bc6SPL set ID 6daf1ebe-b0a2-4413-bf25-3de6eb64b0c6RxCUI 199047, 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

N483324000850 followed by a unit qualifier and the quantity

Package 83324-0008-50. 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 Mar 27, 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 83324-008

What is NDC 83324-008?: 83324-008 is the product NDC for famotidine, Famotidine 20 mg/1 tablet, film coated, listed with the FDA by CHAIN DRUG MARKETING ASSOCIATION, INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: famotidine.
What is the active ingredient?: Famotidine.
Who is the labeler?: CHAIN DRUG MARKETING ASSOCIATION, INC., NDC labeler code 83324. 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?: 252 other product NDCs are listed under this name. See all famotidine 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 NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Famotidine	Famotidine 40 mg/5mL	Powder, For suspensionOral	NorthStar Rx LLC	72603-564	72603-0564-01
Famotidine	Famotidine 40 mg/5mL	Powder, For suspensionOral	RISING PHARMA HOLDINGS, INC.	64980-737	64980-0737-50
Famotidine	Famotidine 40 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-4144	68788-4144-0368788-4144-0468788-4144-06+1 more
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0589	80425-0589-0180425-0589-0280425-0589-03
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Family Dollar Stores, LLC	55319-057	55319-0057-1055319-0057-2555319-0057-50
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Unit Dose Solutions, Inc.	87441-030	87441-0030-01
Famotidine	Famotidine 20 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4119	68788-4119-0168788-4119-0368788-4119-04+3 more
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Safecor Health, LLC	48433-150	48433-0150-20
Famotidine	Famotidine 20 mg/1	Tablet, CoatedOral	Preferred Pharmaceuticals Inc.	68788-4088	68788-4088-0368788-4088-0468788-4088-06+1 more
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4574	70518-4574-0070518-4574-0170518-4574-02+1 more

All 253 famotidine NDCs

Other NDCs under ANDA 215766

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

FDA NDC Directory listings under ANDA 215766
Product	Strength	Form · route	Labeler	Product NDC
famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Camber Consumer Care Inc	69230-326
Famotidine	Famotidine 10 mg/10mg	TabletOral	Little Pharma, Inc.	72559-038
famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	CHAIN DRUG MARKETING ASSOCIATION, INC.	83324-003
Goodmeds Famotidine 20mg 500 countfamotidine 20mg	Famotidine 20 mg/1	TabletOral	Cabinet Health P.B.C.	82725-4047
Heartburn Relieffamotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Shield Pharmaceuticals Corp	83059-0031