NDC codes

FDA NDC Directory
Product NDC (as listed)70729-002Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70729-0002Add 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
70729-002-24707290002247072900022424 TABLET in 1 BOTTLE (70729-002-24)Marketed from Mar 1, 1999
70729-002-50707290002507072900025050 TABLET in 1 BOTTLE (70729-002-50)Marketed from Mar 1, 1999

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)
Dye Free Ibuprofen
Generic name (nonproprietary)
ibuprofen
Active ingredients
Ibuprofen — 200 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Breeden Brothers, LLCNDC labeler code 70729
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075139
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 70729-002_e7bbd188-5e3e-4f1c-96d8-53f6de4b3120SPL ID e7bbd188-5e3e-4f1c-96d8-53f6de4b3120SPL set ID ba106f6f-2c6b-4c98-a10e-d27622b08b25RxCUI 310965UNII WK2XYI10QM

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

N470729000224 followed by a unit qualifier and the quantity

Package 70729-0002-24. 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 _ temporarily relieves minor aches and pains due to: _ backache _ muscular aches _ minor pain of arthritis _ headache _ menstrual cramps _ toothache _ the common cold _ temporarily reduces fever Drug Facts (continued)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70729-002

What is NDC 70729-002?
70729-002 is the product NDC for Dye Free Ibuprofen (ibuprofen), Ibuprofen 200 mg/1 tablet, listed with the FDA by Breeden Brothers, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Dye Free Ibuprofen (Ibuprofen).
What is the active ingredient?
Ibuprofen.
Who is the labeler?
Breeden Brothers, LLC, NDC labeler code 70729. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Dye Free Ibuprofen?
4 other product NDCs are listed under this name. See all Dye Free 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 Dye Free Ibuprofen NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Dye-Free IbuprofenibuprofenIbuprofen 200 mg/1201Capsule, Liquid filledOralCHAIN DRUG MARKETING ASSOCIATION INC.63868-80563868-0805-40
Dye-Free IbuprofenibuprofenIbuprofen 200 mg/1201Capsule, Liquid filledOralRITE AID CORPORATION11822-187911822-1879-01
Dye Free IbuprofenibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralWalgreen Company0363-043800363-0438-3200363-0438-9800363-0438-99
Dye Free IbuprofenibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralWalgreen Company0363-438100363-4381-12

Other NDCs under ANDA 075139

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

FDA NDC Directory listings under ANDA 075139
ProductStrengthForm · routeLabelerProduct NDC
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-0669
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralTopco Associates, LLC36800-993
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralCardinal Health 110, LLC. DBA Leader70000-0291
Ibuprofen Dye-FreeibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralWal-Mart Stores Inc49035-438
Ibuprofen Dye FreeibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralWALMART INC.79903-415
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralH E B37808-393
pain relief ibuprofenibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralRite Aid Corporation11822-0392
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralRite Aid Corporation11822-0393
Dye Free IbuprofenibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralWalgreen Company0363-4381
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralMeijer Distribution Inc41250-993
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralARMY AND AIR FORCE EXCHANGE SERVICE55301-392
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-7914
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralCOSTCO WHOLESALE CORPORATION63981-393
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralARMY AND AIR FORCE EXCHANGE SERVICE55301-393
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralMeijer Distribution, Inc.79481-0392
Dye Free IbuprofenibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralWalgreen Company0363-0438
Ibuprofen Dye FreeibuprofenIbuprofen 200 mg/1Tablet, Film coatedOralCVS Pharmacy59779-438
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralFamily Dollar Services Inc55319-893
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralL.N.K. International, Inc.50844-353
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralL.N.K. International, Inc.50844-352

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