NDC codes

FDA NDC Directory
Product NDC (as listed)71993-313Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71993-0313Add 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
71993-313-107199303131071993031310100 CAPSULE in 1 BOTTLE (71993-313-10)Marketed from May 15, 2026

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 — 200 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Atland Pharmaceuticals, LLCNDC labeler code 71993
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 71993-313_51ac5c0c-2aef-abe1-e063-6294a90a7943SPL ID 51ac5c0c-2aef-abe1-e063-6294a90a7943SPL set ID b26c8351-a955-4685-adad-a7233db39d92RxCUI 197694UNII 0X2CW1QABJ

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

N471993031310 followed by a unit qualifier and the quantity

Package 71993-0313-10. 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)

1. INDICATIONS AND USAGE 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)

About NDC 71993-313

What is NDC 71993-313?
71993-313 is the product NDC for Fenoprofen calcium, Fenoprofen calcium 200 mg/1 capsule, listed with the FDA by Atland Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Fenoprofen calcium.
What is the active ingredient?
Fenoprofen calcium.
Who is the labeler?
Atland Pharmaceuticals, LLC, NDC labeler code 71993. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Fenoprofen calcium?
9 other product NDCs are listed under this name. See all Fenoprofen calcium 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 Fenoprofen calcium NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Fenoprofen CalciumFenoprofen calcium 300 mg/1CapsuleOralCoral Way Pharma, LLC85437-50285437-0502-10
Fenoprofen CalciumFenoprofen calcium 200 mg/1CapsuleOralRising Pharma Holdings, Inc.16571-88616571-0886-01
Fenoprofen CalciumFenoprofen calcium 300 mg/1CapsuleOralRising Pharma Holdings, Inc.16571-88716571-0887-01
Fenoprofen CalciumFenoprofen calcium 400 mg/1CapsuleOralAtland Pharmaceuticals, LLC71993-30871993-0308-90
Fenoprofen CalciumFenoprofen calcium 200 mg/1CapsuleOralMisemer Pharmaceuticals, Inc.0276-050100276-0501-10
Fenoprofen CalciumFenoprofen calcium 300 mg/1CapsuleOralMisemer Pharmaceuticals, Inc.0276-050200276-0502-10
Fenoprofen CalciumFenoprofen calcium 400 mg/1CapsuleOralMisemer Pharmaceuticals, Inc.0276-050300276-0503-90
Fenoprofen CalciumFenoprofen calcium 400 mg/1CapsuleOralRising Pharma Holdings, Inc.16571-68816571-0688-09
Fenoprofen CalciumFenoprofen calcium 400 mg/1CapsuleOralProficient Rx LP71205-82871205-0828-3071205-0828-6071205-0828-90

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 400 mg/1CapsuleOralRising Pharma Holdings, Inc.16571-688
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/1CapsuleOralProficient Rx LP71205-828
Fenoprofen CalciumFenoprofen calcium 400 mg/1CapsuleOralAtland Pharmaceuticals, LLC71993-308
Fenopron Tmfenoprofen calciumFenoprofen calcium 300 mg/1CapsuleOralGalt Pharmaceuticals, LLC61825-311

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