NDC codes

FDA NDC Directory
Product NDC (as listed)0682-0150Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00682-0150Add 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
0682-0150-600068201506060 CAPSULE in 1 BOTTLE (0682-0150-60)Marketed from Apr 2, 2026

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Ketoprofen
Generic name (nonproprietary)
ketoprofen
Active ingredients
Ketoprofen — 75 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 074014
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 0682-0150_4e7bceb6-dcb6-c5e0-e063-6294a90a101eSPL ID 4e7bceb6-dcb6-c5e0-e063-6294a90a101eSPL set ID 4e7bceb6-dcb5-c5e0-e063-6294a90a101eRxCUI 197856UNII 90Y4QC304K

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

N400682015060 followed by a unit qualifier and the quantity

Package 00682-0150-60. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 074014

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

FDA NDC Directory listings under ANDA 074014
ProductStrengthForm · routeLabelerProduct NDC
OrudisketoprofenKetoprofen 75 mg/1CapsuleOralAllegis Pharmaceuticals, Inc.28595-031
KetoprofenKetoprofen 25 mg/1CapsuleOralMisemer Pharmaceuticals, Inc.0276-0504
KetoprofenKetoprofen 50 mg/1CapsuleOralMisemer Pharmaceuticals, Inc.0276-0506
KetoprofenKetoprofen 75 mg/1CapsuleOralMisemer Pharmaceuticals, Inc.0276-0507
KetoprofenKetoprofen 50 mg/1CapsuleOralOncora Pharma, LLC85477-111

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free Med-Code account to keep looking up NDCs, J-codes and drugs.

Create a free accountLog in