NDC codes

FDA NDC Directory
Product NDC (as listed)68071-3786Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-3786Add 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
68071-3786-3680713786036807137860330 TABLET, FILM COATED in 1 BOTTLE (68071-3786-3)Marketed from Jan 29, 2025
68071-3786-6680713786066807137860660 TABLET, FILM COATED in 1 BOTTLE (68071-3786-6)Marketed from Sep 16, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
NuCare Pharmaceuticals, Inc.NDC labeler code 68071
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215767
Marketing start
Listing expires
Other FDA classes
Histamine H2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 68071-3786_5b9dabaa-dd52-0b29-e063-6294a90a9ff2SPL ID 5b9dabaa-dd52-0b29-e063-6294a90a9ff2

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

N468071378603 followed by a unit qualifier and the quantity

Package 68071-3786-03. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 68071-3786

What is NDC 68071-3786?
68071-3786 is the product NDC for Famotidine, Famotidine 20 mg/1 tablet, film coated, listed with the FDA by NuCare Pharmaceuticals, Inc.. It has 2 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?
NuCare Pharmaceuticals, Inc., NDC labeler code 68071. 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 215767

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

FDA NDC Directory listings under ANDA 215767
ProductStrengthForm · routeLabelerProduct NDC
Acid ReducerfamotidineFamotidine 20 mg/1TabletOralAllegiant Health69168-445
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-017
FamotidineFamotidine 40 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-018
FamotidineFamotidine 40 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6790
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7178
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7180
FamotidineFamotidine 40 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7196
FamotidineFamotidine 40 mg/1Tablet, Film coatedOralST. MARY'S MEDICAL PARK PHARMACY60760-937
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralRedpharm Drug67296-2264
FamotidineFamotidine 40 mg/1Tablet, Film coatedOralRedpharm Drug67296-2330
FamotidineFamotidine 40 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals, Inc.68788-8733
FamotidineFamotidine 40 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2527
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-331
FamotidineFamotidine 40 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-427
FamotidineFamotidine 40 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-589
FamotidineFamotidine 20 mg/1Tablet, Film coatedOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0329

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