What is NDC 71930-022?

71930-022 is the product NDC for Oxycodone Hydrochloride, Oxycodone hydrochloride 5 mg/5mL solution, listed with the FDA by Eywa Pharma Inc. It has 1 package NDC, shown above in 10- and 11-digit form.

Eywa Pharma Inc, NDC labeler code 71930. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Oxycodone Hydrochloride?

130 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Oxycodone Hydrochloride NDC 71930-022

NDC codes

FDA NDC Directory

Product NDC (as listed)71930-022Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71930-0022Add 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 NDC	11-digit (billing)	Package	Copy
71930-022-43	7193000224371930002243	1 BOTTLE in 1 CARTON (71930-022-43) / 473 mL in 1 BOTTLEMarketed from Mar 1, 2019

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 Hydrochloride
Generic name (nonproprietary): oxycodone hydrochloride
Active ingredients: Oxycodone hydrochloride — 5 mg/5mL
Dosage form: Solution
Route: Oral
Labeler: Eywa Pharma IncNDC labeler code 71930
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207511
Marketing start: Mar 1, 2019
Listing expires: Dec 31, 2027
DEA schedule: CII
Other FDA classes: Full Opioid Agonists (Mechanism)
Identifiers: Product ID 71930-022_d5dbbf3c-6269-488c-b3a2-9539f45e3945SPL ID d5dbbf3c-6269-488c-b3a2-9539f45e3945SPL set ID 685f409f-946f-4b7e-8130-5ad7b92a5e7aRxCUI 1049604UNII 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

N471930002243 followed by a unit qualifier and the quantity

Package 71930-0022-43. 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.

About NDC 71930-022

What is NDC 71930-022?: 71930-022 is the product NDC for Oxycodone Hydrochloride, Oxycodone hydrochloride 5 mg/5mL solution, listed with the FDA by Eywa Pharma Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Oxycodone Hydrochloride.
What is the active ingredient?: Oxycodone hydrochloride.
Who is the labeler?: Eywa Pharma Inc, NDC labeler code 71930. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Oxycodone Hydrochloride?: 130 other product NDCs are listed under this name. See all Oxycodone Hydrochloride 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 Oxycodone Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Oxycodone Hydrochloride	Oxycodone hydrochloride 15 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-967	60760-0967-3060760-0967-60
Oxycodone Hydrochloride	Oxycodone hydrochloride 10 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-966	60760-0966-3060760-0966-60
Oxycodone Hydrochloride	Oxycodone hydrochloride 5 mg/1	TabletOral	Camber Pharmaceuticals Inc	31722-484	31722-0484-0131722-0484-05
Oxycodone Hydrochloride	Oxycodone hydrochloride 10 mg/1	TabletOral	Camber Pharmaceuticals Inc	31722-485	31722-0485-0131722-0485-05
Oxycodone Hydrochloride	Oxycodone hydrochloride 20 mg/1	TabletOral	Camber Pharmaceuticals Inc	31722-486	31722-0486-0131722-0486-05
Oxycodone Hydrochloride	Oxycodone hydrochloride 5 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-954	60760-0954-3060760-0954-60
Oxycodone Hydrochloride	Oxycodone hydrochloride 15 mg/1	TabletOral	ST. MARY'S MEDICAL PARK PHARMACY	60760-956	60760-0956-3060760-0956-6060760-0956-90
Oxycodone Hydrochloride	Oxycodone hydrochloride 5 mg/1	TabletOral	Strides Pharma Science Limited	64380-259	64380-0259-0164380-0259-02
Oxycodone Hydrochloride	Oxycodone hydrochloride 10 mg/1	TabletOral	Strides Pharma Science Limited	64380-260	64380-0260-01
Oxycodone Hydrochloride	Oxycodone hydrochloride 15 mg/1	TabletOral	Strides Pharma Science Limited	64380-261	64380-0261-0164380-0261-02

All 131 Oxycodone Hydrochloride NDCs

Other NDCs under ANDA 207511

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

FDA NDC Directory listings under ANDA 207511
Product	Strength	Form · route	Labeler	Product NDC
Oxycodone Hydrochloride	Oxycodone hydrochloride 5 mg/5mL	SolutionOral	MAJOR PHARMACEUTICALS	0904-6678
Oxycodone Hydrochloride	Oxycodone hydrochloride 5 mg/5mL	SolutionOral	MAJOR PHARMACEUTICALS	0904-6828
Oxycodone Hydrochloride	Oxycodone hydrochloride 5 mg/5mL	SolutionOral	Bryant Ranch Prepack	63629-1174