NDC codes

FDA NDC Directory
Product NDC (as listed)43598-907Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43598-0907Add 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
43598-907-56435980907564359809075656 TABLET, FILM COATED in 1 BOTTLE (43598-907-56)Marketed from Dec 13, 2024

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 tartrate
Generic name (nonproprietary)
varenicline tartrate
Active ingredients
Varenicline tartrate — .5 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Dr. Reddys Laboratories Inc.NDC labeler code 43598
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215931
Marketing start
Listing expires
Other FDA classes
Cholinergic Agonists (Mechanism)Partial Cholinergic Nicotinic Agonists (Mechanism)
Identifiers
Product ID 43598-907_65233c50-9a25-15c3-cc2b-98713a8173b2SPL ID 65233c50-9a25-15c3-cc2b-98713a8173b2SPL set ID 16ee0a83-88d7-97de-1e07-f9e6dcb5c934RxCUI 636671, 636676, 749289, 749788UNII 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

N443598090756 followed by a unit qualifier and the quantity

Package 43598-0907-56. 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 are 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 43598-907

What is NDC 43598-907?
43598-907 is the product NDC for varenicline tartrate, Varenicline tartrate .5 mg/1 tablet, film coated, listed with the FDA by Dr. Reddys Laboratories Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
varenicline tartrate.
What is the active ingredient?
Varenicline tartrate.
Who is the labeler?
Dr. Reddys Laboratories Inc., NDC labeler code 43598. 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 tartrate?
21 other product NDCs are listed under this name. See all varenicline tartrate 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 tartrate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
varenicline tartrateVarenicline tartrate .5 mg/1Tablet, Film coatedOralMicro Labs Limited42571-45942571-0459-82
varenicline tartrateVarenicline tartrate 1 mg/1Tablet, Film coatedOralMicro Labs Limited42571-46042571-0460-8242571-0460-88
Varenicline tartrate—KitMicro Labs Limited42571-47542571-0475-84
varenicline tartrate—KitOralDr. Reddys Laboratories Inc.43598-02243598-0022-56
varenicline tartrate—KitOralDr. Reddys Laboratories Inc.43598-02343598-0023-53
varenicline tartrateVarenicline tartrate 1 mg/1Tablet, Film coatedOralDr. Reddys Laboratories Inc.43598-90843598-0908-56
Varenicline tartrateVarenicline tartrate .5 mg/1Tablet, Film coatedOralIndoco Remedies Limited14445-15314445-0153-56
Varenicline tartrateVarenicline tartrate 1 mg/1Tablet, Film coatedOralIndoco Remedies Limited14445-15414445-0154-0214445-0154-56
Varenicline tartrateVarenicline tartrate .5 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-799650090-7996-00
Varenicline tartrateVarenicline tartrate .5 mg/1Tablet, Film coatedOralFlorida Pharmaceutical Products, LLC71921-30871921-0308-56

All 22 varenicline tartrate NDCs

Other NDCs under ANDA 215931

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

FDA NDC Directory listings under ANDA 215931
ProductStrengthForm · routeLabelerProduct NDC
varenicline tartrate—KitOralDr. Reddys Laboratories Inc.43598-022
varenicline tartrate—KitOralDr. Reddys Laboratories Inc.43598-023
varenicline tartrateVarenicline tartrate 1 mg/1Tablet, Film coatedOralDr. Reddys Laboratories Inc.43598-908

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