NDC codes

FDA NDC Directory
Product NDC (as listed)70677-1171Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70677-1171Add 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
70677-1171-170677117101100 BLISTER PACK in 1 CARTON (70677-1171-1) / 1 GUM, CHEWING in 1 BLISTER PACKMarketed from Apr 20, 2024

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
Foster and Thrive Nicotine
Generic name (nonproprietary)
nicotine polacrilex
Active ingredients
Nicotine — 4 mg/1
Dosage form
Gum, Chewing
Route
Oral
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076779
Marketing start
Listing expires
Other FDA classes
Nicotine (Chemical structure)
Identifiers
Product ID 70677-1171_27304aa6-ef10-40f5-a135-4974b7a6a7dcSPL ID 27304aa6-ef10-40f5-a135-4974b7a6a7dcSPL set ID 23d8c1a7-a1e4-488d-bc66-b22683abf08bRxCUI 311975UNII 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

N470677117101 followed by a unit qualifier and the quantity

Package 70677-1171-01. 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)

Other NDCs under ANDA 076779

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

FDA NDC Directory listings under ANDA 076779
ProductStrengthForm · routeLabelerProduct NDC
Nicotinenicotine polacrilexNicotine 4 mg/1Gum, ChewingOralMeijer Distribution Inc41250-532
quitine nicotinenicotine polacrilexNicotine 4 mg/1Gum, ChewingOralQUITINE LLC84720-532
Equate nicotinenicotine polacrilexNicotine 4 mg/1Gum, ChewingOralWal-Mart Stores Inc49035-532
Topcare Nicotinenicotine polacrilexNicotine 4 mg/1Gum, ChewingOralTopco Associates LLC36800-532
basic care nicotinenicotine polacrilexNicotine 4 mg/1Gum, ChewingOralAmazon.com Services LLC72288-532
Nicotinenicotine polacrilexNicotine 4 mg/1Gum, ChewingOralRite Aid Corporation11822-0699
Nicotinenicotine polacrilexNicotine 4 mg/1Gum, ChewingOralWalgreen Company0363-0919
Nicotinenicotine polacrilexNicotine 4 mg/1Gum, ChewingOralH E B37808-658
dg health nicotinenicotine polacrilexNicotine 4 mg/1Gum, ChewingOralDolgencorp Inc55910-122
Up and Up Nicotinenicotine polacrilexNicotine 4 mg/1Gum, ChewingOralTarget Corporation82442-532
Good Sense Nicotinenicotine polacrilexNicotine 4 mg/1Gum, ChewingOralL. Perrigo Company0113-0532

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