NDC codes

FDA NDC Directory
Product NDC (as listed)49884-156Labeler and product segments. Claims need a package NDC.
Product NDC at billing width49884-0156Add 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
49884-156-76498840156764988401567656 TABLET, FILM COATED in 1 BOTTLE (49884-156-76)Marketed from Sep 21, 2021

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
Par Health USA, LLCNDC labeler code 49884
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 201785
Marketing start
Listing expires
Other FDA classes
Cholinergic Agonists (Mechanism)Partial Cholinergic Nicotinic Agonists (Mechanism)
Identifiers
Product ID 49884-156_f703e1ca-8acc-4b42-ac8a-4a90b749cbe7SPL ID f703e1ca-8acc-4b42-ac8a-4a90b749cbe7SPL set ID 9e5c0ef3-3179-4d7b-bc76-901473c73ce8RxCUI 636671, 636676, 749289UNII 82269ASB48UPC 0349884155766, 0349884156763, 0349884944995
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

N449884015676 followed by a unit qualifier and the quantity

Package 49884-0156-76. 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 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 49884-156

What is NDC 49884-156?
49884-156 is the product NDC for Varenicline (varenicline tartrate), Varenicline tartrate 1 mg/1 tablet, film coated, listed with the FDA by Par Health USA, LLC. 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?
Par Health USA, LLC, NDC labeler code 49884. 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 tartrateVarenicline tartrate 1 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-89360687-0893-21
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

All 57 Varenicline NDCs

Other NDCs under ANDA 201785

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

FDA NDC Directory listings under ANDA 201785
ProductStrengthForm · routeLabelerProduct NDC
Vareniclinevarenicline tartrateVarenicline tartrate .5 mg/1Tablet, Film coatedOralPar Health USA, LLC49884-155
Vareniclinevarenicline tartrate—KitPar Health USA, LLC49884-944
Vareniclinevarenicline tartrateVarenicline tartrate 1 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-648

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