NDC codes

FDA NDC Directory
Product NDC (as listed)71205-828Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71205-0828Add 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
71205-828-307120508283030 CAPSULE in 1 BOTTLE (71205-828-30)Marketed from Aug 15, 2023
71205-828-607120508286060 CAPSULE in 1 BOTTLE (71205-828-60)Marketed from Aug 15, 2023
71205-828-907120508289090 CAPSULE in 1 BOTTLE (71205-828-90)Marketed from Aug 15, 2023

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)
Fenoprofen Calcium
Generic name (nonproprietary)
fenoprofen calcium
Active ingredients
Fenoprofen calcium — 400 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214475
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 71205-828_1d438989-6431-4c62-8f24-444475d423a3SPL ID 1d438989-6431-4c62-8f24-444475d423a3SPL set ID 1d438989-6431-4c62-8f24-444475d423a3RxCUI 858116UNII 0X2CW1QABJUPC 0371205828905

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

N471205082830 followed by a unit qualifier and the quantity

Package 71205-0828-30. 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)

Fenoprofen calcium is indicated for: • Relief of mild to moderate pain in adults • Relief of the signs and symptoms of rheumatoid arthritis • Relief of the signs and symptoms of osteoarthritis Fenoprofen calcium is a nonsteroidal anti-inflammatory drug indicated for: • Relief of mild to moderate pain in adults. ( 1 ) • Relief of the signs and symptoms of rheumatoid arthritis. ( 1 ) • Relief of the signs and symptoms of osteoarthritis. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 214475

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

FDA NDC Directory listings under ANDA 214475
ProductStrengthForm · routeLabelerProduct NDC
Fenoprofen CalciumFenoprofen calcium 200 mg/1CapsuleOralRising Pharma Holdings, Inc.16571-886
Fenoprofen CalciumFenoprofen calcium 300 mg/1CapsuleOralRising Pharma Holdings, Inc.16571-887
Fenoprofen CalciumFenoprofen calcium 400 mg/1CapsuleOralAtland Pharmaceuticals, LLC71993-308
Fenoprofen calciumFenoprofen calcium 200 mg/1CapsuleOralAtland Pharmaceuticals, LLC71993-313
Fenopron Tmfenoprofen calciumFenoprofen calcium 300 mg/1CapsuleOralGalt Pharmaceuticals, LLC61825-311
Fenoprofen CalciumFenoprofen calcium 400 mg/1CapsuleOralRising Pharma Holdings, Inc.16571-688

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