NDC codes

FDA NDC Directory
Product NDC (as listed)72559-013Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72559-0013Add 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
72559-013-11725590013116 BLISTER PACK in 1 CARTON (72559-013-11) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMarketed from Jul 23, 2021
72559-013-2372559001323300 TABLET, EXTENDED RELEASE in 1 BOTTLE (72559-013-23)Marketed from Sep 15, 2026
72559-013-2872559001328150 TABLET, EXTENDED RELEASE in 1 BOTTLE (72559-013-28)Marketed from Apr 6, 2022
72559-013-41725590013412 BOTTLE in 1 PACKAGE, COMBINATION (72559-013-41) / 150 TABLET, EXTENDED RELEASE in 1 BOTTLEMarketed from Jul 23, 2021
72559-013-647255900136484 TABLET, EXTENDED RELEASE in 1 BOTTLE (72559-013-64)Marketed from Nov 15, 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)
Curist Mucus Relief Maximum StrengthSuffix: Maximum Strength
Generic name (nonproprietary)
guaifenesin
Active ingredients
Guaifenesin — 1200 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Labeler
Little Pharma, Inc.NDC labeler code 72559
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213420
Marketing start
Listing expires
Other FDA classes
Decreased Respiratory Secretion Viscosity (Physiologic effect)Increased Respiratory Secretions (Physiologic effect)
Identifiers
Product ID 72559-013_59d14f50-a21c-58ca-e063-6394a90a1e8aSPL ID 59d14f50-a21c-58ca-e063-6394a90a1e8aSPL set ID c7d1136c-a712-2ac5-e053-2995a90a4dd4RxCUI 310621UNII 495W7451VQUPC 0372559013238
Pharmacologic class
Expectorant

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

N472559001311 followed by a unit qualifier and the quantity

Package 72559-0013-11. 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)

Uses helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72559-013

What is NDC 72559-013?
72559-013 is the product NDC for Curist Mucus Relief Maximum Strength, Guaifenesin 1200 mg/1 tablet, extended release, listed with the FDA by Little Pharma, Inc.. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Curist Mucus Relief Maximum Strength (Guaifenesin).
What is the active ingredient?
Guaifenesin.
Who is the labeler?
Little Pharma, Inc., NDC labeler code 72559. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Curist Mucus Relief Maximum Strength?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under ANDA 213420

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

FDA NDC Directory listings under ANDA 213420
ProductStrengthForm · routeLabelerProduct NDC
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralAAA Pharmaceutical, Inc.57344-203
Good Sense Mucus ERguaifenesinGuaifenesin 1200 mg/1Tablet, Multilayer, Extended releaseOralL. Perrigo Company0113-3650
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralNUVICARE LLC84324-026
Mucus ReliefguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralNUVICARE LLC84324-034
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralAdvanced Rx LLC80513-403
GuaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralAdvanced Rx LLC80513-413
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralHYVEE INC42507-253
Mucus ReliefguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralPioneer Life Sciences, LLC72090-012
GuaifenesinGuaifenesin 600 mg/1TabletOralTARGET CORPORATION11673-539
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralPioneer Life Sciences, LLC72090-011
GuaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralCVS PHARMACY, INC69842-335
Betr chest congestion reliefguaifenesinGuaifenesin 1200 mg/1Tablet, Multilayer, Extended releaseOralLive Betr LLC80267-002
Betr remedies chest congestion reliefguaifenesinGuaifenesin 1200 mg/1Tablet, Multilayer, Extended releaseOralLive Betr LLC80267-010
Topcare Mucus ERguaifenesinGuaifenesin 1200 mg/1Tablet, Multilayer, Extended releaseOralTopco Associates LLC76162-523
GuaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralGranules India Ltd62207-570
GuaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralGRANULES PHARMACEUTICALS INC.70010-199
GuaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralGranules India Ltd62207-569
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralDemoulas Super Markets, Inc53942-203
Mucus Relief Maximum StrengthguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralDemoulas Super Markets, Inc53942-204
basic care mucus er maxguaifenesinGuaifenesin 1200 mg/1Tablet, Multilayer, Extended releaseOralAmazon.com Services LLC72288-650

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