NDC codes

FDA NDC Directory
Product NDC (as listed)76420-322Labeler and product segments. Claims need a package NDC.
Product NDC at billing width76420-0322Add 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
76420-322-0176420032201100 TABLET in 1 BOTTLE (76420-322-01)Marketed from Apr 15, 2025
76420-322-0576420032205500 TABLET in 1 BOTTLE (76420-322-05)Marketed from Apr 15, 2025
76420-322-307642003223030 TABLET in 1 BOTTLE (76420-322-30)Marketed from Apr 15, 2025
76420-322-607642003226060 TABLET in 1 BOTTLE (76420-322-60)Marketed from Apr 15, 2025
76420-322-907642003229090 TABLET in 1 BOTTLE (76420-322-90)Marketed from Apr 15, 2025

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)
Oxycodone And Acetaminophen
Generic name (nonproprietary)
oxycodone and acetaminophen
Active ingredients
Oxycodone hydrochloride7.5 mg/1Acetaminophen325 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207419
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Full Opioid Agonists (Mechanism)
Identifiers
Product ID 76420-322_32cd8c6c-83cf-fa16-e063-6394a90a6f38SPL ID 32cd8c6c-83cf-fa16-e063-6394a90a6f38SPL set ID 71c7a627-6ed9-4f49-8cdc-b3228c021e64RxCUI 1049214, 1049221, 1049225, 1049635UNII 362O9ITL9D, C1ENJ2TE6C
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

N476420032201 followed by a unit qualifier and the quantity

Package 76420-0322-01. 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

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

Indications (excerpt from the label)

INDICATIONS AND USAGE Oxycodone and Acetaminophen Tablets are indicated for the management of pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate. Limitations of Use Because of the risks of addiction, abuse, and misuse, with opioids, which can occur at any dosage or duration [see Warnings] , reserve Oxycodone and Acetaminophen Tablets for use in patients for whom alternative treatment options (e.g., non-opioid analgesics): Have not been tolerated or are not expected to be tolerated, Have not provided adequate analgesia or are not expected to provide adequate analgesia Oxycodone and Acetaminophen Tablets should not be used for an extended peri

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 207419

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

FDA NDC Directory listings under ANDA 207419
ProductStrengthForm · routeLabelerProduct NDC
Oxycodone And AcetaminophenOxycodone hydrochloride 10 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack71335-2106
Oxycodone And AcetaminophenOxycodone hydrochloride 10 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack63629-8834
Oxycodone and AcetaminophenOxycodone hydrochloride 5 mg/1; Acetaminophen 325 mg/1TabletOralProficient Rx LP71205-329
Oxycodone and AcetaminophenOxycodone hydrochloride 10 mg/1; Acetaminophen 325 mg/1TabletOralProficient Rx LP71205-347
Oxycodone And AcetaminophenOxycodone hydrochloride 5 mg/1; Acetaminophen 325 mg/1TabletOralBryant Ranch Prepack63629-8888
Oxycodone and AcetaminophenOxycodone hydrochloride 5 mg/1; Acetaminophen 325 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-5169
Oxycodone And AcetaminophenOxycodone hydrochloride 2.5 mg/1; Acetaminophen 325 mg/1TabletOralAsclemed USA, Inc.76420-320
Oxycodone And AcetaminophenOxycodone hydrochloride 5 mg/1; Acetaminophen 325 mg/1TabletOralAsclemed USA, Inc.76420-321
Oxycodone And AcetaminophenOxycodone hydrochloride 10 mg/1; Acetaminophen 325 mg/1TabletOralAsclemed USA, Inc.76420-323
Oxycodone And AcetaminophenOxycodone hydrochloride 2.5 mg/1; Acetaminophen 325 mg/1TabletOralXLCare Pharmaceuticals, Inc.72865-113
Oxycodone And AcetaminophenOxycodone hydrochloride 5 mg/1; Acetaminophen 325 mg/1TabletOralXLCare Pharmaceuticals, Inc.72865-114
Oxycodone And AcetaminophenOxycodone hydrochloride 7.5 mg/1; Acetaminophen 325 mg/1TabletOralXLCare Pharmaceuticals, Inc.72865-115
Oxycodone And AcetaminophenOxycodone hydrochloride 10 mg/1; Acetaminophen 325 mg/1TabletOralXLCare Pharmaceuticals, Inc.72865-116
Oxycodone and AcetaminophenOxycodone hydrochloride 7.5 mg/1; Acetaminophen 325 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-193
Oxycodone and AcetaminophenOxycodone hydrochloride 2.5 mg/1; Acetaminophen 325 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-191
Oxycodone and AcetaminophenOxycodone hydrochloride 5 mg/1; Acetaminophen 325 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-192
Oxycodone and AcetaminophenOxycodone hydrochloride 10 mg/1; Acetaminophen 325 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-194
Oxycodone And AcetaminophenOxycodone hydrochloride 7.5 mg/1; Acetaminophen 325 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-950
Oxycodone And AcetaminophenOxycodone hydrochloride 2.5 mg/1; Acetaminophen 325 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-948
Oxycodone And AcetaminophenOxycodone hydrochloride 5 mg/1; Acetaminophen 325 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-949

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