NDC codes

FDA NDC Directory
Product NDC (as listed)87063-117Labeler and product segments. Claims need a package NDC.
Product NDC at billing width87063-0117Add 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
87063-117-0187063011701100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-01)Marketed from Feb 16, 2026
87063-117-0587063011705500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-05)Marketed from Feb 16, 2026
87063-117-108706301171010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-10)Marketed from Feb 16, 2026
87063-117-208706301172020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-20)Marketed from Feb 16, 2026
87063-117-308706301173030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-30)Marketed from Feb 16, 2026
87063-117-508706301175050 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-50)Marketed from Feb 16, 2026
87063-117-608706301176060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-60)Marketed from Feb 16, 2026
87063-117-908706301179090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-90)Marketed from Feb 16, 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)
Tramadol Hydrochloride
Generic name (nonproprietary)
tramadol hydrochloride
Active ingredients
Tramadol hydrochloride — 50 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211825
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Full Opioid Agonists (Mechanism)
Identifiers
Product ID 87063-117_4aea6bdc-3282-556d-e063-6394a90afb0cSPL ID 4aea6bdc-3282-556d-e063-6394a90afb0cSPL set ID 18d9e3e4-5892-43b8-b211-3ef3393ad946RxCUI 835603UNII 9N7R477WCK
Pharmacologic class
Opioid Agonist

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

N487063011701 followed by a unit qualifier and the quantity

Package 87063-0117-01. 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

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

Other NDCs under ANDA 211825

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

FDA NDC Directory listings under ANDA 211825
ProductStrengthForm · routeLabelerProduct NDC
Tramadol HydrochlorideTramadol hydrochloride 50 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-4035
Tramadol HydrochlorideTramadol hydrochloride 50 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-4040
Tramadol HydrochlorideTramadol hydrochloride 50 mg/1Tablet, Film coatedOralAdvanced Rx of Tennessee, LLC80425-0548
Tramadol HydrochlorideTramadol hydrochloride 50 mg/1Tablet, Film coatedOralUnichem Pharmaceuticals (USA), Inc.29300-355
Tramadol HydrochlorideTramadol hydrochloride 50 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-5789
Tramadol HydrochlorideTramadol hydrochloride 50 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-5790

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