NDC codes

FDA NDC Directory
Product NDC (as listed)0135-0511Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00135-0511Add 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
0135-0511-01001350511013 CONTAINER in 1 CARTON (0135-0511-01) / 24 LOZENGE in 1 CONTAINERMarketed from Oct 19, 2010
0135-0511-06001350511061 CONTAINER in 1 CARTON (0135-0511-06) / 24 LOZENGE in 1 CONTAINERMarketed from Sep 1, 2015
0135-0511-07001350511076 CONTAINER in 1 CARTON (0135-0511-07) / 24 LOZENGE in 1 CONTAINERMarketed from Sep 1, 2015

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Nicorette
Generic name (nonproprietary)
nicotine polacrilex
Active ingredients
Nicotine — 4 mg/1
Dosage form
Lozenge
Route
Oral
Labeler
Haleon US Holdings LLCNDC labeler code 0135
Product type
Over-the-counter drug
Marketing category
NDA — New Drug ApplicationApplication NDA 021330
Marketing start
Listing expires
Other FDA classes
Nicotine (Chemical structure)
Identifiers
Product ID 0135-0511_142b2250-8264-423f-e063-6394a90ab05bSPL ID 142b2250-8264-423f-e063-6394a90ab05bSPL set ID 991704ed-781a-489b-8b56-0b558e8fc385RxCUI 359817, 359818, 968849, 968851UNII 6M3C89ZY6R
Pharmacologic class
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

N400135051101 followed by a unit qualifier and the quantity

Package 00135-0511-01. 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 .

Indications (excerpt from the label)

Use reduces withdrawal symptoms, including nicotine craving, associated with quitting smoking

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0135-0511

What is NDC 0135-0511?
0135-0511 is the product NDC for Nicorette (nicotine polacrilex), Nicotine 4 mg/1 lozenge, listed with the FDA by Haleon US Holdings LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Nicorette (Nicotine polacrilex).
What is the active ingredient?
Nicotine.
Who is the labeler?
Haleon US Holdings LLC, NDC labeler code 0135. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Nicorette?
8 other product NDCs are listed under this name. See all Nicorette 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 Nicorette NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Nicorettenicotine polacrilexNicotine 2 mg/1LozengeOralHaleon US Holdings LLC0135-063500135-0635-01
Nicorettenicotine polacrilexNicotine 4 mg/1LozengeOralHaleon US Holdings LLC0135-063600135-0636-01
Nicorettenicotine polacrilexNicotine 4 mg/1LozengeOralHaleon US Holdings LLC0135-150000135-1500-0100135-1500-02
Nicorettenicotine polacrilexNicotine 2 mg/1LozengeOralHaleon US Holdings LLC0135-280000135-2800-0100135-2800-02
Nicorettenicotine polacrilexNicotine 2 mg/1LozengeOralHaleon US Holdings LLC0135-062500135-0625-0100135-0625-0200135-0625-03
Nicorettenicotine polacrilexNicotine 4 mg/1LozengeOralHaleon US Holdings LLC0135-062600135-0626-0100135-0626-0200135-0626-03
Nicorettenicotine polacrilexNicotine 2 mg/1LozengeOralHaleon US Holdings LLC0135-051000135-0510-0100135-0510-0600135-0510-07
Nicorettenicotine polacrilexNicotine 2 mg/1LozengeOralHaleon US Holdings LLC0135-050800135-0508-0200135-0508-0300135-0508-04

Other NDCs under NDA 021330

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

FDA NDC Directory listings under NDA 021330
ProductStrengthForm · routeLabelerProduct NDC
Nicorettenicotine polacrilexNicotine 2 mg/1LozengeOralHaleon US Holdings LLC0135-0510
Nicorettenicotine polacrilexNicotine 2 mg/1LozengeOralHaleon US Holdings LLC0135-0625
Nicorettenicotine polacrilexNicotine 4 mg/1LozengeOralHaleon US Holdings LLC0135-0626

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