NDC codes

FDA NDC Directory
Product NDC (as listed)58602-706Labeler and product segments. Claims need a package NDC.
Product NDC at billing width58602-0706Add 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 NDC11-digit (billing)PackageCopy
58602-706-1458602070614586020706141 BOTTLE in 1 CARTON (58602-706-14) / 50 TABLET, FILM COATED in 1 BOTTLEMarketed from Apr 26, 2016
58602-706-1558602070615586020706152 BLISTER PACK in 1 CARTON (58602-706-15) / 8 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Feb 24, 2020
58602-706-1658602070616586020706161 BOTTLE in 1 CARTON (58602-706-16) / 65 TABLET, FILM COATED in 1 BOTTLEMarketed from Apr 26, 2016
58602-706-1858602070618586020706181 BOTTLE in 1 CARTON (58602-706-18) / 80 TABLET, FILM COATED in 1 BOTTLEMarketed from Apr 26, 2016
58602-706-1958602070619586020706191 BOTTLE in 1 CARTON (58602-706-19) / 90 TABLET, FILM COATED in 1 BOTTLEMarketed from Jan 8, 2021
58602-706-2158602070621586020706211 BOTTLE in 1 CARTON (58602-706-21) / 100 TABLET, FILM COATED in 1 BOTTLEMarketed from Apr 26, 2016
58602-706-3458602070634586020706341 BOTTLE in 1 CARTON (58602-706-34) / 200 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 22, 2020
58602-706-3958602070639586020706391 BOTTLE in 1 CARTON (58602-706-39) / 365 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 22, 2020
58602-706-4058602070640586020706401 BOTTLE in 1 CARTON (58602-706-40) / 500 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 22, 2020
58602-706-4158602070641586020706411000 TABLET, FILM COATED in 1 BOTTLE (58602-706-41)Marketed from Sep 4, 2020
58602-706-4458602070644586020706441 BOTTLE in 1 CARTON (58602-706-44) / 400 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 22, 2020
58602-706-4758602070647586020706471 BOTTLE in 1 CARTON (58602-706-47) / 75 TABLET, FILM COATED in 1 BOTTLEMarketed from Apr 26, 2016
58602-706-5058602070650586020706501 BOTTLE in 1 CARTON (58602-706-50) / 85 TABLET, FILM COATED in 1 BOTTLEMarketed from Apr 26, 2016
58602-706-5358602070653586020706531 BOTTLE in 1 CARTON (58602-706-53) / 25 TABLET, FILM COATED in 1 BOTTLEMarketed from Apr 26, 2016
58602-706-5458602070654586020706541 BOTTLE in 1 CARTON (58602-706-54) / 70 TABLET, FILM COATED in 1 BOTTLEMarketed from Apr 26, 2016
58602-706-5658602070656586020706561 BOTTLE in 1 CARTON (58602-706-56) / 35 TABLET, FILM COATED in 1 BOTTLEMarketed from Apr 26, 2016
58602-706-6258602070662586020706625 BLISTER PACK in 1 CARTON (58602-706-62) / 5 TABLET, FILM COATED in 1 BLISTER PACK (58602-706-60)Marketed from Apr 26, 2016
58602-706-7958602070679586020706791 BLISTER PACK in 1 CARTON (58602-706-79) / 8 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Apr 26, 2016
58602-706-885860207068858602070688750 TABLET, FILM COATED in 1 BOTTLE (58602-706-88)Marketed from Jul 22, 2020
58602-706-945860207069458602070694100 TABLET, FILM COATED in 1 BOTTLE (58602-706-94)Marketed from Apr 26, 2016

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
Listing expires
Other FDA classes
Histamine H2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 58602-706_4329025b-5cdd-4287-955f-028e6aca198cSPL ID 4329025b-5cdd-4287-955f-028e6aca198cSPL set ID f2b911c7-ce24-4d3d-8fb6-c34980191f40RxCUI 310273UNII 5QZO15J2Z8

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

N458602070614 followed by a unit qualifier and the quantity

Package 58602-0706-14. 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 .

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 58602-706

What is NDC 58602-706?
58602-706 is the product NDC for Famotidine, Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Aurohealth LLC. It has 20 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?
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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
FamotidineFamotidine 40 mg/5mLPowder, For suspensionOralNorthStar Rx LLC72603-56472603-0564-01
FamotidineFamotidine 40 mg/5mLPowder, For suspensionOralRISING PHARMA HOLDINGS, INC.64980-73764980-0737-50
FamotidineFamotidine 40 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-414468788-4144-0368788-4144-0468788-4144-06+1 more
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralAdvanced Rx of Tennessee, LLC80425-058980425-0589-0180425-0589-0280425-0589-03
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralFamily Dollar Stores, LLC55319-05755319-0057-1055319-0057-2555319-0057-50
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralUnit Dose Solutions, Inc.87441-03087441-0030-01
FamotidineFamotidine 20 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-411968788-4119-0168788-4119-0368788-4119-04+3 more
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralSafecor Health, LLC48433-15048433-0150-20
FamotidineFamotidine 20 mg/1Tablet, CoatedOralPreferred Pharmaceuticals Inc.68788-408868788-4088-0368788-4088-0468788-4088-06+1 more
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-457470518-4574-0070518-4574-0170518-4574-02+1 more

All 253 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
ProductStrengthForm · routeLabelerProduct NDC
Amazon Basic Care Acid ReducerfamotidineFamotidine 20 mg/1Tablet, Film coatedOralAmazon.com Services LLC72288-363
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralWALGREEN CO.0363-1899
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralWALGREEN CO.0363-4400
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralWALGREEN CO.0363-5300
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralWALGREEN CO.0363-9607
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralBetter Living Brands, LLC21130-033
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralBetter Living Brands LLC21130-039
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralAmerisource Bergen46122-735
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralAmerisource Bergen46122-737
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralWal-Mart Stores, Inc.49035-505
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralWal-Mart Stores, Inc.49035-589
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralMagno-Humphries, Inc.54257-180
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralMagno-Humphries, Inc.54257-802
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralFred's, Inc.55315-435
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralFamily Dollar Stores, LLC55319-057
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralAurohealth LLC58602-705
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralAurohealth LLC58602-828
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralAurohealth LLC58602-829
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralAurohealth LLC58602-859
FamotidineFamotidine 10 mg/1Tablet, Film coatedOralBest Choice63941-009

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