NDC codes

FDA NDC Directory
Product NDC (as listed)60687-935Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60687-0935Add 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
60687-935-216068709352130 BLISTER PACK in 1 CARTON (60687-935-21) / 1 TABLET in 1 BLISTER PACK (60687-935-11)Marketed from Feb 18, 2026

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)
Ticagrelor
Generic name (nonproprietary)
ticagrelor
Active ingredients
Ticagrelor — 60 mg/1
Dosage form
Tablet
Route
Oral
Labeler
American Health PackagingNDC labeler code 60687
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208596
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 3A4 Inhibitors (Mechanism)Decreased Platelet Aggregation (Physiologic effect)P-Glycoprotein Inhibitors (Mechanism)P2Y12 Receptor Antagonists (Mechanism)
Identifiers
Product ID 60687-935_5c4fa8e7-a6a8-45d8-e063-6294a90af6deSPL ID 5c4fa8e7-a6a8-45d8-e063-6294a90af6de
Pharmacologic class
P2Y12 Platelet Inhibitor

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

N460687093521 followed by a unit qualifier and the quantity

Package 60687-0935-21. 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

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

About NDC 60687-935

What is NDC 60687-935?
60687-935 is the product NDC for Ticagrelor, Ticagrelor 60 mg/1 tablet, listed with the FDA by American Health Packaging. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ticagrelor.
What is the active ingredient?
Ticagrelor.
Who is the labeler?
American Health Packaging, NDC labeler code 60687. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ticagrelor?
51 other product NDCs are listed under this name. See all Ticagrelor 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 Ticagrelor NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
TicagrelorTicagrelor 90 mg/1TabletOralLaurus Labs Limited42385-99442385-0994-0142385-0994-0542385-0994-11+4 more
TicagrelorTicagrelor 60 mg/1TabletOralLaurus Labs Limited42385-99342385-0993-0142385-0993-0542385-0993-11+4 more
TicagrelorTicagrelor 60 mg/1Tablet, Film coatedOralNorthStar RxLLC72603-94072603-0940-01
TicagrelorTicagrelor 90 mg/1Tablet, Film coatedOralNorthStar RxLLC72603-94172603-0941-0172603-0941-02
TicagrelorTicagrelor 60 mg/1TabletOralAiPing Pharmaceutical, Inc11788-15711788-0157-60
TicagrelorTicagrelor 90 mg/1TabletOralAiPing Pharmaceutical, Inc11788-15811788-0158-0111788-0158-60
TicagrelorTicagrelor 90 mg/1Tablet, Film coatedOralLifestar Pharma LLC70756-04870756-0048-6070756-0048-99
TicagrelorTicagrelor 60 mg/1Tablet, Film coatedOralLifestar Pharma LLC70756-04770756-0047-60
TicagrelorTicagrelor 60 mg/1TabletOralOryza Pharmaceuticals, Inc.72516-01772516-0017-06
TicagrelorTicagrelor 90 mg/1TabletOralAmerican Health Packaging60687-92860687-0928-57

All 52 Ticagrelor NDCs

Other NDCs under ANDA 208596

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

FDA NDC Directory listings under ANDA 208596
ProductStrengthForm · routeLabelerProduct NDC
TicagrelorTicagrelor 60 mg/1TabletOralAvKARE73190-003
TicagrelorTicagrelor 90 mg/1TabletOralAvKARE73190-008
TicagrelorTicagrelor 90 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC53401-028
TicagrelorTicagrelor 90 mg/1TabletOralAvPAK50268-826
TicagrelorTicagrelor 90 mg/1TabletOralAmerican Health Packaging60687-928
TicagrelorTicagrelor 90 mg/1TabletOralNovadoz Pharmaceuticals LLC72205-368
TicagrelorTicagrelor 60 mg/1TabletOralNovadoz Pharmaceuticals LLC72205-406

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Ticagrelor NDC 60687-935 | National Drug Code | Med-Code