NDC codes

FDA NDC Directory
Product NDC (as listed)70771-1980Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70771-1980Add 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
70771-1980-17077119800170771198001100 TABLET in 1 BOTTLE (70771-1980-1)Marketed from Feb 27, 2026
70771-1980-3707711980037077119800330 TABLET in 1 BOTTLE (70771-1980-3)Marketed from Feb 27, 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)
Dapsone
Generic name (nonproprietary)
dapsone
Active ingredients
Dapsone — 100 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Zydus Lifesciences LimitedNDC labeler code 70771
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 220103
Marketing start
Listing expires
Other FDA classes
Sulfones (Chemical structure)
Identifiers
Product ID 70771-1980_a4ce6655-3e02-434d-87ad-5bcec90202c1SPL ID a4ce6655-3e02-434d-87ad-5bcec90202c1SPL set ID 1d6bc112-ba2f-40ab-975d-9cfbc853cd11RxCUI 197557, 197558UNII 8W5C518302
Pharmacologic class
Sulfone

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

N470771198001 followed by a unit qualifier and the quantity

Package 70771-1980-01. 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 .

Full label on DailyMed (opens in a new tab)

About NDC 70771-1980

What is NDC 70771-1980?
70771-1980 is the product NDC for Dapsone, Dapsone 100 mg/1 tablet, listed with the FDA by Zydus Lifesciences Limited. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Dapsone.
What is the active ingredient?
Dapsone.
Who is the labeler?
Zydus Lifesciences Limited, NDC labeler code 70771. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Dapsone?
45 other product NDCs are listed under this name. See all Dapsone 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 Dapsone NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
DapsoneDapsone 25 mg/1TabletOralMacleods Pharmaceuticals Limited33342-53433342-0534-0733342-0534-11
DapsoneDapsone 100 mg/1TabletOralMacleods Pharmaceuticals Limited33342-53533342-0535-0733342-0535-11
DapsoneDapsone 50 mg/gGelTopicalAlembic Pharmaceuticals Limited46708-55146708-0551-3046708-0551-6046708-0551-90
DapsoneDapsone 50 mg/gGelTopicalAlembic Pharmaceuticals Inc.62332-55162332-0551-3062332-0551-6062332-0551-90
DapsoneDapsone 25 mg/1TabletOralZydus Lifesciences Limited70771-197970771-1979-0170771-1979-03
DapsoneDapsone 25 mg/1TabletOralViona Pharmaceuticals Inc72578-17772578-0177-0172578-0177-06
DapsoneDapsone 100 mg/1TabletOralViona Pharmaceuticals Inc72578-17872578-0178-0172578-0178-06
DapsoneDapsone 25 mg/1TabletOralAvKARE73190-03773190-0037-01
DapsoneDapsone 25 mg/1TabletOralWestminster Pharmaceuticals, LLC69367-40969367-0409-0169367-0409-30
DapsoneDapsone 100 mg/1TabletOralWestminster Pharmaceuticals, LLC69367-41069367-0410-0169367-0410-30

All 46 Dapsone NDCs

Other NDCs under ANDA 220103

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

FDA NDC Directory listings under ANDA 220103
ProductStrengthForm · routeLabelerProduct NDC
DapsoneDapsone 25 mg/1TabletOralZydus Lifesciences Limited70771-1979
DapsoneDapsone 25 mg/1TabletOralViona Pharmaceuticals Inc72578-177
DapsoneDapsone 100 mg/1TabletOralViona Pharmaceuticals Inc72578-178

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