NDC codes

FDA NDC Directory
Product NDC (as listed)60687-893Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60687-0893Add 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
60687-893-21606870893216068708932130 BLISTER PACK in 1 CARTON (60687-893-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-893-11)Marketed from Dec 9, 2025

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)
Varenicline
Generic name (nonproprietary)
varenicline tartrate
Active ingredients
Varenicline tartrate — 1 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
American Health PackagingNDC labeler code 60687
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213019
Marketing start
Listing expires
Other FDA classes
Cholinergic Agonists (Mechanism)Partial Cholinergic Nicotinic Agonists (Mechanism)
Identifiers
Product ID 60687-893_459a090a-2b6b-2bff-e063-6294a90a5c7cSPL ID 459a090a-2b6b-2bff-e063-6294a90a5c7cSPL set ID 38be1217-cd55-416a-bf4b-6ede6bfd3727RxCUI 636676UNII 82269ASB48
Pharmacologic class
Cholinergic Receptor Agonist; Partial Cholinergic Nicotinic Agonist

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

N460687089321 followed by a unit qualifier and the quantity

Package 60687-0893-21. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Varenicline tablets are indicated for use as an aid to smoking cessation treatment. Varenicline tablets is a nicotinic receptor partial agonist indicated for use as an aid to smoking cessation treatment. (1 and 2.1)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60687-893

What is NDC 60687-893?
60687-893 is the product NDC for Varenicline (varenicline tartrate), Varenicline tartrate 1 mg/1 tablet, film coated, 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?
Varenicline (Varenicline tartrate).
What is the active ingredient?
Varenicline tartrate.
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 Varenicline?
56 other product NDCs are listed under this name. See all Varenicline 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 Varenicline NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Vareniclinevarenicline tartrateVarenicline tartrate .5 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-464770518-4647-00
VareniclineVarenicline tartrate .5 mg/1TabletOralUmedica Laboratories USA Inc.60290-07760290-0077-0160290-0077-02
VareniclineVarenicline tartrate 1 mg/1TabletOralUmedica Laboratories USA Inc.60290-07860290-0078-0160290-0078-0260290-0078-03
varenicline—KitUmedica Laboratories USA Inc.60290-09560290-0095-01
VareniclineVarenicline tartrate .5 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-41759651-0417-56
VareniclineVarenicline tartrate 1 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-41859651-0418-5559651-0418-56
Varenicline—KitAurobindo Pharma Limited59651-45159651-0451-53
Vareniclinevarenicline tartrateVarenicline tartrate .5 mg/1Tablet, Film coatedOralMarlex Pharmaceuticals, Inc.10135-80810135-0808-56
Vareniclinevarenicline tartrateVarenicline tartrate 1 mg/1Tablet, Film coatedOralMarlex Pharmaceuticals, Inc.10135-80910135-0809-56
VareniclineVarenicline tartrate .5 mg/1Tablet, Film coatedOralMacleods Pharmaceuticals Limited33342-48933342-0489-19

All 57 Varenicline NDCs

Other NDCs under ANDA 213019

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

FDA NDC Directory listings under ANDA 213019
ProductStrengthForm · routeLabelerProduct NDC
Vareniclinevarenicline tartrateVarenicline tartrate .5 mg/1Tablet, Film coatedOralAjanta Pharma USA Inc.27241-173
Vareniclinevarenicline tartrateVarenicline tartrate 1 mg/1Tablet, Film coatedOralAjanta Pharma USA Inc.27241-174
Vareniclinevarenicline tartrate—KitAjanta Pharma USA Inc.27241-187

Free account

Log in to keep searching

You’ve used your 3 free searches. Med-Code is free: log in or create a free profile to keep looking up NDCs, J-codes and drugs.

Create a free profileLog in