Prescription drug · ANDA

Tapentadol Hydrochloride NDC 73190-083

Tapentadol hydrochloride 100 mg/1 · Tablet, Film coated · Oral · AvKARE

NDC codes

FDA NDC Directory
Product NDC (as listed)73190-083Labeler and product segments. Claims need a package NDC.
Product NDC at billing width73190-0083Add 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
73190-083-0173190008301100 TABLET, FILM COATED in 1 BOTTLE (73190-083-01)Marketed from Sep 14, 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)
Tapentadol Hydrochloride
Generic name (nonproprietary)
tapentadol hydrochloride
Active ingredients
Tapentadol hydrochloride — 100 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
AvKARE
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 220865
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Opioid Agonists (Mechanism)
Identifiers
Product ID 73190-083_5b769a8c-f810-3f17-e063-6294a90a2cedSPL ID 5b769a8c-f810-3f17-e063-6294a90a2ced
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

N473190008301 followed by a unit qualifier and the quantity

Package 73190-0083-01. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 220865

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

FDA NDC Directory listings under ANDA 220865
ProductStrengthForm · routeLabelerProduct NDC
Tapentadol HydrochlorideTapentadol hydrochloride 75 mg/1Tablet, Film coatedOralAvKARE73190-082
Tapentadol HydrochlorideTapentadol hydrochloride 50 mg/1Tablet, Film coatedOralAvKARE73190-081
Tapentadol HydrochlorideTapentadol hydrochloride 50 mg/1Tablet, Film coatedOralNovadoz Pharmaceuticals LLC72205-369
Tapentadol HydrochlorideTapentadol hydrochloride 75 mg/1Tablet, Film coatedOralNovadoz Pharmaceuticals LLC72205-370
Tapentadol HydrochlorideTapentadol hydrochloride 100 mg/1Tablet, Film coatedOralNovadoz Pharmaceuticals LLC72205-371

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Tapentadol Hydrochloride NDC 73190-083 | Med-Code