What is NDC 58602-829?

58602-829 is the product NDC for Famotidine, Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Aurohealth LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.

Aurohealth LLC, NDC labeler code 58602. 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?

254 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 58602-829 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)58602-829Labeler and product segments. Claims need a package NDC.

Product NDC at billing width58602-0829Add 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
58602-829-21	58602082921	1 BOTTLE in 1 CARTON (58602-829-21) / 100 TABLET, FILM COATED in 1 BOTTLEMarketed from Apr 26, 2016
58602-829-34	58602082934	1 BOTTLE in 1 CARTON (58602-829-34) / 200 TABLET, FILM COATED in 1 BOTTLEMarketed from Mar 25, 2021
58602-829-50	58602082950	1 BOTTLE in 1 CARTON (58602-829-50) / 85 TABLET, FILM COATED in 1 BOTTLEMarketed from Mar 2, 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 — 20 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Aurohealth LLCNDC labeler code 58602
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 206531
Marketing start: Apr 26, 2016
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 58602-829_2c043b30-86e8-4c8a-b247-d9b6e72a3dbcSPL ID 2c043b30-86e8-4c8a-b247-d9b6e72a3dbcSPL set ID 5b161f25-c578-4ff4-a931-ff3a1e681c50RxCUI 310273UNII 5QZO15J2Z8UPC 0358602829216
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

N458602082921 followed by a unit qualifier and the quantity

Package 58602-0829-21. 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 4, 2026.

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 58602-829

What is NDC 58602-829?: 58602-829 is the product NDC for Famotidine, Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Aurohealth LLC. 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?: Aurohealth LLC, NDC labeler code 58602. 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?: 254 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 255 Famotidine NDCs

Other NDCs under ANDA 206531

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

FDA NDC Directory listings under ANDA 206531
Product	Strength	Form · route	Labeler	Product NDC
Amazon Basic Care Acid Reducerfamotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Amazon.com Services LLC	72288-363
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	WALGREEN CO.	0363-1899
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	WALGREEN CO.	0363-4400
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	WALGREEN CO.	0363-5300
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	WALGREEN CO.	0363-9607
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Better Living Brands, LLC	21130-033
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Better Living Brands LLC	21130-039
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Amerisource Bergen	46122-735
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Amerisource Bergen	46122-737
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Wal-Mart Stores, Inc.	49035-505
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Wal-Mart Stores, Inc.	49035-589
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Magno-Humphries, Inc.	54257-180
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Magno-Humphries, Inc.	54257-802
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Fred's, Inc.	55315-435
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Family Dollar Stores, LLC	55319-057
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Aurohealth LLC	58602-705
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Aurohealth LLC	58602-706
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Aurohealth LLC	58602-828
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Aurohealth LLC	58602-859
Famotidine	Famotidine 10 mg/1	Tablet, Film coatedOral	Best Choice	63941-009

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