What is NDC 69230-326?

69230-326 is the product NDC for famotidine, Famotidine 10 mg/1 tablet, film coated, listed with the FDA by Camber Consumer Care Inc. It has 5 package NDCs, shown above in 10- and 11-digit form.

Camber Consumer Care Inc, NDC labeler code 69230. 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 69230-326 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)69230-326Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69230-0326Add 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
69230-326-01	6923003260169230032601	1 BOTTLE in 1 CARTON (69230-326-01) / 100 TABLET, FILM COATED in 1 BOTTLEMarketed from Nov 8, 2021
69230-326-05	6923003260569230032605	1 BOTTLE in 1 CARTON (69230-326-05) / 500 TABLET, FILM COATED in 1 BOTTLEMarketed from Nov 8, 2021
69230-326-10	6923003261069230032610	1 BOTTLE in 1 CARTON (69230-326-10) / 1000 TABLET, FILM COATED in 1 BOTTLEMarketed from Nov 8, 2021
69230-326-30	6923003263069230032630	1 BOTTLE in 1 CARTON (69230-326-30) / 30 TABLET, FILM COATED in 1 BOTTLEMarketed from Nov 8, 2021
69230-326-60	6923003266069230032660	1 BOTTLE in 1 CARTON (69230-326-60) / 60 TABLET, FILM COATED in 1 BOTTLEMarketed from Nov 8, 2021

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 — 10 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Camber Consumer Care IncNDC labeler code 69230
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 215766
Marketing start: Nov 8, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 69230-326_eabd2ff8-a7d9-2ac4-e053-2995a90a3b40SPL ID eabd2ff8-a7d9-2ac4-e053-2995a90a3b40SPL set ID ebe3ca30-df25-4c56-8935-414a3431b5b9RxCUI 199047, 310273UNII 5QZO15J2Z8UPC 0369230326305, 0369230327302, 0369230327012, 0369230326015
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

N469230032601 followed by a unit qualifier and the quantity

Package 69230-0326-01. 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 Oct 11, 2022.

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 69230-326

What is NDC 69230-326?: 69230-326 is the product NDC for famotidine, Famotidine 10 mg/1 tablet, film coated, listed with the FDA by Camber Consumer Care Inc. It has 5 package NDCs, 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?: Camber Consumer Care Inc, NDC labeler code 69230. 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/10mg	TabletOral	Little Pharma, Inc.	72559-038
famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	CHAIN DRUG MARKETING ASSOCIATION, INC.	83324-003
famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	CHAIN DRUG MARKETING ASSOCIATION, INC.	83324-008
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