NDC codes

FDA NDC Directory
Product NDC (as listed)30142-604Labeler and product segments. Claims need a package NDC.
Product NDC at billing width30142-0604Add 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
30142-604-6230142060462301420604621 BOTTLE in 1 CARTON (30142-604-62) / 24 TABLET, FILM COATED in 1 BOTTLEMarketed from Jan 15, 1988

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)
ibuprofen
Generic name (nonproprietary)
ibuprofen
Active ingredients
Ibuprofen — 200 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Kroger CompanyNDC labeler code 30142
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 072096
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 30142-604_3593df8b-c7dd-47d6-804a-27a5b35f93cfSPL ID 3593df8b-c7dd-47d6-804a-27a5b35f93cf

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

N430142060462 followed by a unit qualifier and the quantity

Package 30142-0604-62. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 30142-604

What is NDC 30142-604?
30142-604 is the product NDC for ibuprofen, Ibuprofen 200 mg/1 tablet, film coated, 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?
ibuprofen.
What is the active ingredient?
Ibuprofen.
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 ibuprofen?
672 other product NDCs are listed under this name. See all ibuprofen 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 ibuprofen NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-480170518-4801-00
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-478470518-4784-0070518-4784-01
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-478670518-4786-00
IbuprofenIbuprofen 200 mg/1TabletOralFamora Inc87509-000487509-0004-05
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralMedcore LLC82461-72482461-0724-90
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralMedcore LLC82461-72582461-0725-90
IbuprofenIbuprofen 200 mg/1TabletOralAurohealth LLC58602-91358602-0913-1758602-0913-40
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-73767877-0737-0167877-0737-0567877-0737-33+1 more
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-73867877-0738-0167877-0738-0567877-0738-30+3 more
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-73967877-0739-0167877-0739-0567877-0739-30+4 more

All 673 ibuprofen NDCs

Other NDCs under ANDA 072096

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

FDA NDC Directory listings under ANDA 072096
ProductStrengthForm · routeLabelerProduct NDC
up and up ibuprofenibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralTarget Corporation11673-604
ibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralUnit Dose Solutions, Inc.87441-043
Topcare IbuprofenibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralTopco Associates LLC36800-647
good sense ibuprofenibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralL. Perrigo Company0113-0647
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralRite Aid Corporation11822-6604
Berkley and Jensen IbuprofenibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralBJWC68391-604
ibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralProficient Rx LP71205-787
ibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralWalgreen Company0363-0604
basic care ibuprofenibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralAmazon.com Services LLC72288-311
ibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-6747
Signature Care IbuprofenibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralSafeway21130-818
ibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralH E B37808-647
equaline ibuprofenibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralUnited Natural Foods, Inc. dba UNFI41163-604
kirkland signature ibuprofenibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralCostco Wholesale Company63981-604
ibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-191
equaline ibuprofenibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralUnited Natural Foods, Inc. dba UNFI41163-647
good sense ibuprofenibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2047
good sense ibuprofenibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8590
ibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-7912
Good neighbor pharmacy ibuprofenibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralAmerisource Bergen46122-548

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