What is NDC 70000-0479?

70000-0479 is the product NDC for Mucus Relief Extended Release Maximum Strength, Guaifenesin 1200 mg/1 tablet, listed with the FDA by CARDINAL HEALTH 110, LLC. DBA LEADER 70000. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Mucus Relief Extended Release Maximum Strength (Guaifenesin).

CARDINAL HEALTH 110, LLC. DBA LEADER 70000, NDC labeler code 70000. 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 Extended Release Maximum Strength?

3 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

NDC 70000-0479

NDC codes

FDA NDC Directory

Product NDC (as listed)70000-0479Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70000-0479Add 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 NDC	11-digit (billing)	Package	Copy
70000-0479-1	7000004790170000047901	14 BLISTER PACK in 1 CARTON (70000-0479-1) / 1 TABLET in 1 BLISTER PACKMarketed from Jan 31, 2019
70000-0479-2	7000004790270000047902	28 BLISTER PACK in 1 CARTON (70000-0479-2) / 1 TABLET in 1 BLISTER PACKMarketed from Jan 31, 2019

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): Mucus Relief Extended Release Maximum StrengthSuffix: Maximum Strength
Generic name (nonproprietary): guaifenesin
Active ingredients: Guaifenesin — 1200 mg/1
Dosage form: Tablet
Route: Oral
Labeler: CARDINAL HEALTH 110, LLC. DBA LEADER 70000NDC labeler code 70000
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207342
Marketing start: Jan 31, 2019
Marketing end: Mar 28, 2027
Other FDA classes: Decreased Respiratory Secretion Viscosity (Physiologic effect)Increased Respiratory Secretions (Physiologic effect)
Identifiers: Product ID 70000-0479_df386042-7796-4e24-9f8e-39ea465065adSPL ID df386042-7796-4e24-9f8e-39ea465065adSPL set ID 54a59e95-f95a-4bcd-ac9d-8d4ace85277fRxCUI 310621UNII 495W7451VQUPC 0096295136845
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

N470000047901 followed by a unit qualifier and the quantity

Package 70000-0479-01. 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 Feb 10, 2026.

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 70000-0479

What is NDC 70000-0479?: 70000-0479 is the product NDC for Mucus Relief Extended Release Maximum Strength, Guaifenesin 1200 mg/1 tablet, listed with the FDA by CARDINAL HEALTH 110, LLC. DBA LEADER 70000. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Mucus Relief Extended Release Maximum Strength (Guaifenesin).
What is the active ingredient?: Guaifenesin.
Who is the labeler?: CARDINAL HEALTH 110, LLC. DBA LEADER 70000, NDC labeler code 70000. 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 Extended Release Maximum Strength?: 3 other product NDCs are listed under this name. See all Mucus Relief Extended Release Maximum Strength 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 Extended Release Maximum Strength NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Mucus Relief Extended Release Maximum Strengthguaifenesin	Guaifenesin 1200 mg/1	TabletOral	H E B	37808-762	37808-0762-1437808-0762-42
Mucus Relief Extended Release Maximum Strengthguaifenesin	Guaifenesin 1200 mg/1	TabletOral	CVS Pharmacy	69842-732	69842-0732-1469842-0732-2869842-0732-42
Mucus Relief Extended Release Maximum Strengthguaifenesin	Guaifenesin 1200 mg/1	TabletOral	Walgreens	0363-0832	00363-0832-1400363-0832-28

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
Product	Strength	Form · route	Labeler	Product NDC
Guaifenesin	Guaifenesin 600 mg/1	Tablet, Extended releaseOral	Amneal Pharmaceuticals LLC	65162-036
Guaifenesin	Guaifenesin 1200 mg/1	Tablet, Extended releaseOral	Amneal Pharmaceuticals LLC	65162-037
Mucus Reliefguaifenesin	Guaifenesin 1200 mg/1	Tablet, Extended releaseOral	Rugby Laboratories	0536-1392
Mucus Reliefguaifenesin	Guaifenesin 600 mg/1	TabletOral	Rite Aid Corporation	11822-3252
Mucus Reliefguaifenesin	Guaifenesin 600 mg/1	Tablet, Extended releaseOral	H E B	37808-830
Mucus Reliefguaifenesin	Guaifenesin 600 mg/1	TabletOral	H E B	37808-935
Mucus Reliefguaifenesin	Guaifenesin 600 mg/1	TabletOral	United Natural Foods, Inc. dba UNFI	41163-731
Mucus Reliefguaifenesin	Guaifenesin 1200 mg/1	Tablet, Extended releaseOral	Family Dollar (FAMILY WELLNESS)	55319-551
Mucus Reliefguaifenesin	Guaifenesin 1200 mg/1	Tablet, Extended releaseOral	Family Dollar (FAMILY WELLNESS)	55319-733
Mucus Reliefguaifenesin	Guaifenesin 600 mg/1	TabletOral	Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)	55910-739
Mucus Reliefguaifenesin	Guaifenesin 1200 mg/1	Tablet, Extended releaseOral	P & L Development, LLC	59726-237
Mucus Reliefguaifenesin	Guaifenesin 600 mg/1	Tablet, Extended releaseOral	P & L Development, LLC	59726-734
Mucus Reliefguaifenesin	Guaifenesin 600 mg/1	TabletOral	Best Choice (Valu Merchandisers Company)	63941-731
Mucus Reliefguaifenesin	Guaifenesin 600 mg/1	TabletOral	WinCo Foods, LLC	67091-370
Mucus Reliefguaifenesin	Guaifenesin 600 mg/1	Tablet, Extended releaseOral	Harris Teeter, LLC	69256-731
Mucus Reliefguaifenesin	Guaifenesin 1200 mg/1	Tablet, Extended releaseOral	Strategic Sourcing Services LLC	70677-1051
Mucus Reliefguaifenesin	Guaifenesin 600 mg/1	Tablet, Extended releaseOral	Strategic Sourcing Services LLC	70677-1052
Mucus Relief ERguaifenesin	Guaifenesin 600 mg/1	Tablet, Extended releaseOral	Major Pharmaceuticals	0904-6718
Mucus Relief ERguaifenesin	Guaifenesin 600 mg/1	Tablet, Extended releaseOral	Cardinal Health 107, LLC	55154-4153
Mucus Relief Extended Releaseguaifenesin	Guaifenesin 600 mg/1	Tablet, Extended releaseOral	Rugby Laboratories, Inc.	0536-1163

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Mucus Relief Extended Release Maximum Strength (Guaifenesin) NDC 70000-0479

NDC codes

Product information

Billing references

Product label

About NDC 70000-0479

Other NDCs under ANDA 207342

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NDC codes

Product information

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Product label

About NDC 70000-0479

Related NDCs: other Mucus Relief Extended Release Maximum Strength products

Other NDCs under ANDA 207342