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
0682-0150-60006820150600068201506060 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
Labeler
Marnel Pharmaceuticals, Inc.NDC labeler code 0682
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

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Carefully consider the potential benefits and risks of Ketoprofen Capsules USP and other treatment options before deciding to use Ketoprofen Capsules, USP. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS ). Ketoprofen Capsules, USP is indicated for the management of the signs and symptoms of rheumatoid arthritis and osteoarthritis. Ketoprofen Capsules, USP is indicated for the management of pain. Ketoprofen Capsules, USP indicated for treatment of primary dysmenorrhea.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0682-0150

What is NDC 0682-0150?
0682-0150 is the product NDC for Ketoprofen, Ketoprofen 75 mg/1 capsule, listed with the FDA by Marnel Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ketoprofen.
What is the active ingredient?
Ketoprofen.
Who is the labeler?
Marnel Pharmaceuticals, Inc., NDC labeler code 0682. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ketoprofen?
5 other product NDCs are listed under this name. See all Ketoprofen 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 Ketoprofen NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
KetoprofenKetoprofen 50 mg/1CapsuleOralOncora Pharma, LLC85477-11185477-0111-01
KetoprofenKetoprofen 75 mg/1CapsuleOralMisemer Pharmaceuticals, Inc.0276-050700276-0507-10
KetoprofenKetoprofen 50 mg/1CapsuleOralMisemer Pharmaceuticals, Inc.0276-050600276-0506-10
KetoprofenKetoprofen 25 mg/1CapsuleOralMisemer Pharmaceuticals, Inc.0276-050400276-0504-10
KetoprofenKetoprofen 200 mg/1Capsule, Extended releaseOralMylan Pharmaceuticals Inc.0378-820000378-8200-01

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
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
OrudisketoprofenKetoprofen 75 mg/1CapsuleOralAllegis Pharmaceuticals, Inc.28595-031

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