What is NDC 42385-993?

42385-993 is the product NDC for Ticagrelor, Ticagrelor 60 mg/1 tablet, listed with the FDA by Laurus Labs Limited. It has 7 package NDCs, shown above in 10- and 11-digit form.

Laurus Labs Limited, NDC labeler code 42385. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Ticagrelor NDC 42385-993 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)42385-993Labeler and product segments. Claims need a package NDC.

Product NDC at billing width42385-0993Add 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 NDC	11-digit (billing)	Package
42385-993-01	42385099301	100 TABLET in 1 BOTTLE (42385-993-01)Marketed from Aug 20, 2026
42385-993-05	42385099305	500 TABLET in 1 BOTTLE (42385-993-05)Marketed from Aug 20, 2026
42385-993-11	42385099311	1000 TABLET in 1 BOTTLE (42385-993-11)Marketed from Aug 20, 2026
42385-993-30	42385099330	30 TABLET in 1 BOTTLE (42385-993-30)Marketed from Aug 20, 2026
42385-993-60	42385099360	60 TABLET in 1 BOTTLE (42385-993-60)Marketed from Aug 20, 2026
42385-993-68	42385099368	10 BLISTER PACK in 1 CARTON (42385-993-68) / 10 TABLET in 1 BLISTER PACK (42385-993-10)Marketed from Aug 20, 2026
42385-993-72	42385099372	10 BLISTER PACK in 1 CARTON (42385-993-72) / 10 TABLET in 1 BLISTER PACK (42385-993-17)Marketed from Aug 20, 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: Laurus Labs LimitedNDC labeler code 42385
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 218869
Marketing start: Aug 20, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Cytochrome P450 3A4 Inhibitors (Mechanism)Decreased Platelet Aggregation (Physiologic effect)P-Glycoprotein Inhibitors (Mechanism)P2Y12 Receptor Antagonists (Mechanism)
Identifiers: Product ID 42385-993_555d4e44-9bb2-474e-9bea-c549e3261dbbSPL ID 555d4e44-9bb2-474e-9bea-c549e3261dbbSPL set ID 555d4e44-9bb2-474e-9bea-c549e3261dbbRxCUI 1116635, 1666332UNII GLH0314RVCUPC 0342385994308, 0342385993301
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

N442385099301 followed by a unit qualifier and the quantity

Package 42385-0993-01. 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 Aug 26, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Ticagrelor is a P2Y 12 platelet inhibitor indicated • to reduce the risk of cardiovascular (CV) death, myocardial infarction (MI), and stroke in patients with acute coronary syndrome (ACS) or a history of MI. For at least the first 12 months following ACS, it is superior to clopidogrel. Ticagrelor also reduces the risk of stent thrombosis in patients who have been stented for treatment of ACS. ( 1.1 ) • to reduce the risk of a first MI or stroke in patients with coronary artery disease (CAD) at high risk for such events. While use is not limited to this setting, the efficacy of ticagrelor was established in a population with type 2 diabetes mellitus (T2DM). ( 1.2 ) • to reduce the risk of st…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 42385-993

What is NDC 42385-993?: 42385-993 is the product NDC for Ticagrelor, Ticagrelor 60 mg/1 tablet, listed with the FDA by Laurus Labs Limited. It has 7 package NDCs, 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?: Laurus Labs Limited, NDC labeler code 42385. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Ticagrelor	Ticagrelor 90 mg/1	TabletOral	Laurus Labs Limited	42385-994	42385-0994-0142385-0994-0542385-0994-11+4 more
Ticagrelor	Ticagrelor 60 mg/1	Tablet, Film coatedOral	NorthStar RxLLC	72603-940	72603-0940-01
Ticagrelor	Ticagrelor 90 mg/1	Tablet, Film coatedOral	NorthStar RxLLC	72603-941	72603-0941-0172603-0941-02
Ticagrelor	Ticagrelor 60 mg/1	TabletOral	AiPing Pharmaceutical, Inc	11788-157	11788-0157-60
Ticagrelor	Ticagrelor 90 mg/1	TabletOral	AiPing Pharmaceutical, Inc	11788-158	11788-0158-0111788-0158-60
Ticagrelor	Ticagrelor 60 mg/1	Tablet, Film coatedOral	Lifestar Pharma LLC	70756-047	70756-0047-60
Ticagrelor	Ticagrelor 90 mg/1	Tablet, Film coatedOral	Lifestar Pharma LLC	70756-048	70756-0048-6070756-0048-99
Ticagrelor	Ticagrelor 60 mg/1	TabletOral	American Health Packaging	60687-935	60687-0935-21
Ticagrelor	Ticagrelor 60 mg/1	TabletOral	Oryza Pharmaceuticals, Inc.	72516-017	72516-0017-06
Ticagrelor	Ticagrelor 90 mg/1	TabletOral	American Health Packaging	60687-928	60687-0928-57

All 52 Ticagrelor NDCs

Other NDCs under ANDA 218869

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

FDA NDC Directory listings under ANDA 218869
Product	Strength	Form · route	Labeler	Product NDC
Ticagrelor	Ticagrelor 90 mg/1	TabletOral	Laurus Labs Limited	42385-994