NDC codes

FDA NDC Directory
Product NDC (as listed)68016-801Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68016-0801Add 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
68016-801-2568016080125680160801251 BOTTLE in 1 CARTON (68016-801-25) / 25 TABLET in 1 BOTTLEMarketed from Nov 1, 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
Route
Oral
Labeler
Chain Drug Consortium, LLCNDC labeler code 68016
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077367
Marketing start
Listing expires
Other FDA classes
Histamine H2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 68016-801_b45a96e7-fbe0-e686-e75d-1629dd2cda40SPL ID b45a96e7-fbe0-e686-e75d-1629dd2cda40SPL set ID 937f7bce-955b-9418-5aed-2e84aee50de3RxCUI 199047, 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

N468016080125 followed by a unit qualifier and the quantity

Package 68016-0801-25. 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 68016-801

What is NDC 68016-801?
68016-801 is the product NDC for Famotidine, Famotidine 20 mg/1 tablet, listed with the FDA by Chain Drug Consortium, LLC. 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 Consortium, LLC, NDC labeler code 68016. 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 077367

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

FDA NDC Directory listings under ANDA 077367
ProductStrengthForm · routeLabelerProduct NDC
Acid Reducer Maximum StrengthfamotidineFamotidine 20 mg/1TabletOralDr.Reddys Laboratories Inc.43598-960
Acid Reducer Original StrengthfamotidineFamotidine 10 mg/1TabletOralDr.Reddys Laboratories Inc.43598-824
FamotidineFamotidine 10 mg/1TabletOralAlbertsons Companies21130-022
FamotidineFamotidine 20 mg/1TabletOralAlbertsons Companies21130-023
FamotidineFamotidine 10 mg/1TabletOralDiscount Drug Mart, Inc53943-100
FamotidineFamotidine 20 mg/1TabletOralDiscount Drug Mart, Inc53943-101
FamotidineFamotidine 10 mg/1TabletOralDr.Reddys Laboratories Limited55111-118
FamotidineFamotidine 10 mg/1TabletOralFamily Dollar Stores, Inc.55319-426
FamotidineFamotidine 20 mg/1TabletOralFamily Dollar Stores, Inc.55319-427
FamotidineFamotidine 10 mg/1TabletOralChain Drug Marketing Association INC63868-583
FamotidineFamotidine 20 mg/1TabletOralChain Drug Marketing Association INC63868-584
FamotidineFamotidine 10 mg/1TabletOralChain Drug Consortium, LLC68016-800
FamotidineFamotidine 20 mg/1TabletOralChain Drug Marketing Association INC83324-116
FamotidineFamotidine 10 mg/1TabletOralChain Drug Marketing Association INC83324-139

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