NDC codes

FDA NDC Directory
Product NDC (as listed)70000-0597Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70000-0597Add 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
70000-0597-1700000597011 BOTTLE in 1 CARTON (70000-0597-1) / 50 TABLET in 1 BOTTLEMarketed from May 25, 2022
70000-0597-2700000597021 BOTTLE in 1 CARTON (70000-0597-2) / 100 TABLET in 1 BOTTLEMarketed from May 25, 2022

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)
Ibuprofen
Generic name (nonproprietary)
ibuprofen
Active ingredients
Ibuprofen — 200 mg/1
Dosage form
Tablet
Route
Oral
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 091237
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 70000-0597_dfbbde4f-633e-6d57-e053-2a95a90ad82fSPL ID dfbbde4f-633e-6d57-e053-2a95a90ad82fSPL set ID dfbbde4f-633d-6d57-e053-2a95a90ad82fRxCUI 310965UNII WK2XYI10QMUPC 0096295141870, 0096295141863

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

N470000059701 followed by a unit qualifier and the quantity

Package 70000-0597-01. 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 .

Indications (excerpt from the label)

Uses • temporarily relieves minor aches and pains due to: o headache o muscular aches o minor pain of arthritis o toothache o backache o the common cold o menstrual cramps • temporarily reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 091237

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

FDA NDC Directory listings under ANDA 091237
ProductStrengthForm · routeLabelerProduct NDC
Ibuprofenibuprofen tablets usp, 200mgIbuprofen 200 mg/1TabletOralKROGER COMPANY41226-612
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralTIME CAP LABORATORIES,INC49483-611
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralTIME CAP LABORATORIES,INC49483-612
Ibuprofenibuprofen tablets usp, 200mgIbuprofen 200 mg/1TabletOralBETTER LIVING BRANDS, LLC21130-992
IbuprofenIbuprofen 200 mg/1TabletOralWALGREENS0363-9611
IbuprofenIbuprofen 200 mg/1TabletOralWALGREENS0363-9612
IbuprofenIbuprofen 200 mg/1Tablet, CoatedOralCVS Pharmacy.Inc.69842-489
IbuprofenIbuprofen 200 mg/1TabletOralCVS Pharmacy. Inc.69842-493
IbuprofenIbuprofen 200 mg/1TabletOralMARKSANS PHARMA LIMITED25000-135
IbuprofenIbuprofen 200 mg/1TabletOralMARKSANS PHARMA LIMITED25000-136
IbuprofenIbuprofen 200 mg/1Tablet, CoatedOralTARGET CORPORATION11673-993
IbuprofenIbuprofen 200 mg/1Tablet, CoatedOralRITE AID11822-7893
IbuprofenIbuprofen 200 mg/1Tablet, CoatedOralRITE AID11822-8925

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