NDC codes

FDA NDC Directory
Product NDC (as listed)37808-830Labeler and product segments. Claims need a package NDC.
Product NDC at billing width37808-0830Add 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
37808-830-20378080830201 BOTTLE, PLASTIC in 1 BOX (37808-830-20) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTICMarketed from Jun 5, 2023

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)
Mucus Relief
Generic name (nonproprietary)
guaifenesin
Active ingredients
Guaifenesin — 600 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Labeler
H E BNDC labeler code 37808
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207342
Marketing start
Listing expires
Other FDA classes
Decreased Respiratory Secretion Viscosity (Physiologic effect)Increased Respiratory Secretions (Physiologic effect)
Identifiers
Product ID 37808-830_b74e7c92-7fe7-4455-9af9-6ebe568639b7SPL ID b74e7c92-7fe7-4455-9af9-6ebe568639b7SPL set ID efebda97-5234-451c-a854-91a32303a6b7RxCUI 636522UNII 495W7451VQUPC 0041220831890
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

N437808083020 followed by a unit qualifier and the quantity

Package 37808-0830-20. 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 makes coughs more productive.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 37808-830

What is NDC 37808-830?
37808-830 is the product NDC for Mucus Relief (guaifenesin), Guaifenesin 600 mg/1 tablet, extended release, listed with the FDA by H E B. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Mucus Relief (Guaifenesin).
What is the active ingredient?
Guaifenesin.
Who is the labeler?
H E B, NDC labeler code 37808. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Mucus Relief?
77 other product NDCs are listed under this name. See all Mucus Relief 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 Mucus Relief NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Mucus ReliefguaifenesinGuaifenesin 400 mg/1TabletOralGeri-Care Pharmaceuticals, Corp57896-71857896-0718-01
Mucus ReliefguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralYYBA Corp73581-40373581-0403-0173581-0403-03
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralGrocery Outlet, Inc.85828-72385828-0723-02
mucus reliefguaifenesinGuaifenesin 1200 mg/1Tablet, Multilayer, Extended releaseOralCVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED51316-72851316-0728-5551316-0728-74
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralHYVEE INC42507-25342507-0253-03
Mucus Reliefguaifenesin 400 mgGuaifenesin 400 mg/1TabletOralPioneer Life Sciences, LLC72090-04472090-0044-01
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralPioneer Life Sciences, LLC72090-01172090-0011-0172090-0011-02
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralNUVICARE LLC84324-02684324-0026-01
Mucus ReliefguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralPioneer Life Sciences, LLC72090-01272090-0012-0172090-0012-0272090-0012-03
Mucus ReliefguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralNUVICARE LLC84324-03484324-0034-01

All 78 Mucus Relief NDCs

Other NDCs under ANDA 207342

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

FDA NDC Directory listings under ANDA 207342
ProductStrengthForm · routeLabelerProduct NDC
Mucus ReliefguaifenesinGuaifenesin 600 mg/1TabletOralBest Choice (Valu Merchandisers Company)63941-731
Mucus ReliefguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralFamily Dollar (FAMILY WELLNESS)55319-733
Mucus Relief Extended Release Maximum StrengthguaifenesinGuaifenesin 1200 mg/1TabletOralCVS Pharmacy69842-732
Mucus ReliefguaifenesinGuaifenesin 600 mg/1TabletOralRite Aid Corporation11822-3252
Mucus Relief Extended Release Maximum StrengthguaifenesinGuaifenesin 1200 mg/1TabletOralCARDINAL HEALTH 110, LLC. DBA LEADER 7000070000-0479
Mucus Relief Extended Release Maximum StrengthguaifenesinGuaifenesin 1200 mg/1TabletOralWalgreens0363-0832
Mucus ReliefguaifenesinGuaifenesin 600 mg/1TabletOralH E B37808-935
Mucus Relief Extended ReleaseguaifenesinGuaifenesin 1200 mg/1TabletOralTARGET Corporation11673-732
Mucus ReliefguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralStrategic Sourcing Services LLC70677-1051
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralStrategic Sourcing Services LLC70677-1052
Mucus Relief Extended ReleaseguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralRugby Laboratories, Inc.0536-1163
Mucus Relief ERguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralCardinal Health 107, LLC55154-4153
Mucus Relief Extended ReleaseguaifenesinGuaifenesin 600 mg/1TabletOralCare One (American Sales Company)41520-731
Mucus Relief Maximum StrengthguaifenesinGuaifenesin 1200 mg/1TabletOralCare One (American Sales Company)41520-732
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralHarris Teeter, LLC69256-731
Mucus ReliefguaifenesinGuaifenesin 600 mg/1TabletOralWinCo Foods, LLC67091-370
GuaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralAmneal Pharmaceuticals LLC65162-036
GuaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralAmneal Pharmaceuticals LLC65162-037
Mucus ReliefguaifenesinGuaifenesin 600 mg/1TabletOralDolgencorp, Inc. (DOLLAR GENERAL & REXALL)55910-739
Mucus ReliefguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralP & L Development, LLC59726-237

Showing 20 of 27.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free Med-Code account to keep looking up NDCs, J-codes and drugs.

Create a free accountLog in