What is NDC 55111-119?

55111-119 is the product NDC for Famotidine, Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Dr.Reddy's Laboratories Limited. It has 3 package NDCs, shown above in 10- and 11-digit form.

Dr.Reddy's Laboratories Limited, NDC labeler code 55111. 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 55111-119 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)55111-119Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55111-0119Add 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
55111-119-01	5511101190155111011901	100 TABLET, FILM COATED in 1 BOTTLE (55111-119-01)Marketed from Apr 16, 2001
55111-119-10	5511101191055111011910	1000 TABLET, FILM COATED in 1 BOTTLE (55111-119-10)Marketed from Apr 16, 2001
55111-119-30	5511101193055111011930	30 TABLET, FILM COATED in 1 BOTTLE (55111-119-30)Marketed from Apr 16, 2001

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: Dr.Reddy's Laboratories LimitedNDC labeler code 55111
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 075718
Marketing start: Apr 16, 2001
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 55111-119_b30502a9-c0c8-909c-ec34-956a5e058223SPL ID b30502a9-c0c8-909c-ec34-956a5e058223SPL set ID 06d286ce-14b3-4b66-8b42-ac4a10a0fc90RxCUI 284245, 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

N455111011901 followed by a unit qualifier and the quantity

Package 55111-0119-01. 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 Nov 17, 2020.

Indications (excerpt from the label)

Famotidine tablets are indicated in adult and pediatric patients 40 kg and greater for the treatment of: • active duodenal ulcer (DU). • active gastric ulcer (GU). • symptomatic nonerosive gastroesophageal reflux disease (GERD). • erosive esophagitis due to GERD, diagnosed by biopsy. Famotidine tablets are indicated in adults for the: • treatment of pathological hypersecretory conditions (e.g., Zollinger-Ellison syndrome, multiple endocrine neoplasias). • reduction of the risk of duodenal ulcer recurrence. Famotidine is a histamine-2 (H 2 ) receptor antagonist indicated ( 1 ): In adult and pediatric patients 40 kg and greater for the treatment of: • active duodenal ulcer (DU). • active gastr…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 55111-119

What is NDC 55111-119?: 55111-119 is the product NDC for Famotidine, Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Dr.Reddy's Laboratories Limited. It has 3 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?: Dr.Reddy's Laboratories Limited, NDC labeler code 55111. 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 075718

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

FDA NDC Directory listings under ANDA 075718
Product	Strength	Form · route	Labeler	Product NDC
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Major Pharmaceuticals	0904-7193
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	AvPAK	50268-299
Famotidine	Famotidine 40 mg/1	Tablet, Film coatedOral	Dr.Reddy's Laboratories Limited	55111-120
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-2628
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-4313
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Legacy Pharmaceutical Packaging, LLC	68645-594
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-8889
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-1950
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-543
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Proficient Rx LP	82804-194
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Quality Care Products, LLC	83008-091
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Sportpharm LLC	85766-221
Famotidine	Famotidine 40 mg/1	Tablet, Film coatedOral	Sportpharm LLC	85766-222