NDC codes

FDA NDC Directory
Product NDC (as listed)30142-962Labeler and product segments. Claims need a package NDC.
Product NDC at billing width30142-0962Add 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
30142-962-1430142096214301420962141 BLISTER PACK in 1 CARTON (30142-962-14) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMarketed from Apr 20, 2022

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)
Guaifenesin Extended ReleaseSuffix: Extended Release
Generic name (nonproprietary)
guaifenesin
Active ingredients
Guaifenesin — 1200 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Labeler
Kroger CompanyNDC labeler code 30142
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209254
Marketing start
Listing expires
Other FDA classes
Decreased Respiratory Secretion Viscosity (Physiologic effect)Increased Respiratory Secretions (Physiologic effect)
Identifiers
Product ID 30142-962_7b7122bb-375b-4a86-a494-1dd8995083a9SPL ID 7b7122bb-375b-4a86-a494-1dd8995083a9SPL set ID d434656a-221b-40fc-81ad-2b698be1aa33RxCUI 310621UNII 495W7451VQ
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

N430142096214 followed by a unit qualifier and the quantity

Package 30142-0962-14. 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 30142-962

What is NDC 30142-962?
30142-962 is the product NDC for Guaifenesin Extended Release (guaifenesin), Guaifenesin 1200 mg/1 tablet, extended release, listed with the FDA by Kroger Company. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Guaifenesin Extended Release (Guaifenesin).
What is the active ingredient?
Guaifenesin.
Who is the labeler?
Kroger Company, NDC labeler code 30142. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Guaifenesin Extended Release?
3 other product NDCs are listed under this name. See all Guaifenesin Extended Release 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 Guaifenesin Extended Release NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Guaifenesin Extended-ReleaseguaifenesinGuaifenesin 600 mg/1Tablet, Multilayer, Extended releaseOralPrecision Dose Inc.68094-04868094-0048-61
Guaifenesin Extended ReleaseguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralSAM'S WEST INC68196-99668196-0996-56
Guaifenesin Extended ReleaseguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralPUBLIX SUPER MARKETS, INC41415-99741415-0997-14

Other NDCs under ANDA 209254

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

FDA NDC Directory listings under ANDA 209254
ProductStrengthForm · routeLabelerProduct NDC
GuaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralKroger Company30142-961
GuaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralPublix Super Markets, Inc41415-996
GuaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralAMERISOURCE BERGEN46122-750
GuaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralCVS51316-071
GuaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralOhm Laboratories, Inc.51660-566
GuaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralOhm Laboratories, Inc.51660-567
GuaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralWalmart Stores, Inc.79903-124
Guaifenesin Extended ReleaseguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralPUBLIX SUPER MARKETS, INC41415-997
Guaifenesin Extended ReleaseguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralSAM'S WEST INC68196-996

Free account

Log in to keep searching

You’ve used your 3 free searches. Med-Code is free: log in or create a free profile to keep looking up NDCs, J-codes and drugs.

Create a free profileLog in