What is NDC 87063-039?

87063-039 is the product NDC for Hydromorphone Hydrochloride, Hydromorphone hydrochloride 8 mg/1 tablet, listed with the FDA by ASCLEMED USA INC.. It has 9 package NDCs, shown above in 10- and 11-digit form.

ASCLEMED USA INC., NDC labeler code 87063. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Hydromorphone Hydrochloride?

64 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Hydromorphone Hydrochloride NDC 87063-039

NDC codes

FDA NDC Directory

Product NDC (as listed)87063-039Labeler and product segments. Claims need a package NDC.

Product NDC at billing width87063-0039Add 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
87063-039-01	8706300390187063003901	100 TABLET in 1 BOTTLE, PLASTIC (87063-039-01)Marketed from Dec 4, 2025
87063-039-05	8706300390587063003905	5 TABLET in 1 BOTTLE, PLASTIC (87063-039-05)Marketed from Dec 4, 2025
87063-039-07	8706300390787063003907	7 TABLET in 1 BOTTLE, PLASTIC (87063-039-07)Marketed from Dec 4, 2025
87063-039-10	8706300391087063003910	10 TABLET in 1 BOTTLE, PLASTIC (87063-039-10)Marketed from Dec 4, 2025
87063-039-14	8706300391487063003914	14 TABLET in 1 BOTTLE, PLASTIC (87063-039-14)Marketed from Dec 4, 2025
87063-039-20	8706300392087063003920	20 TABLET in 1 BOTTLE, PLASTIC (87063-039-20)Marketed from Dec 4, 2025
87063-039-30	8706300393087063003930	30 TABLET in 1 BOTTLE, PLASTIC (87063-039-30)Marketed from Dec 4, 2025
87063-039-60	8706300396087063003960	60 TABLET in 1 BOTTLE, PLASTIC (87063-039-60)Marketed from Dec 4, 2025
87063-039-90	8706300399087063003990	90 TABLET in 1 BOTTLE, PLASTIC (87063-039-90)Marketed from Dec 4, 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): Hydromorphone Hydrochloride
Generic name (nonproprietary): hydromorphone hydrochloride
Active ingredients: Hydromorphone hydrochloride — 8 mg/1
Dosage form: Tablet
Route: Oral
Labeler: ASCLEMED USA INC.NDC labeler code 87063
Product type: Prescription drug
Marketing category: NDA authorized genericApplication NDA 019892
Marketing start: Nov 23, 2009
Listing expires: Dec 31, 2026
DEA schedule: CII
Other FDA classes: Full Opioid Agonists (Mechanism)
Identifiers: Product ID 87063-039_451ccd08-4749-97a1-e063-6294a90ac5adSPL ID 451ccd08-4749-97a1-e063-6294a90ac5adSPL set ID 18f6f54e-1537-4181-9d07-54ddf881a9eeRxCUI 897696, 897702, 897710UNII L960UP2KRW
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

N487063003901 followed by a unit qualifier and the quantity

Package 87063-0039-01. 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 Dec 4, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Hydromorphone hydrochloride oral solution and hydromorphone hydrochloride tablets are indicated for the management of pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate. Hydromorphone hydrochloride oral solution and hydromorphone hydrochloride tablets contain hydromorphone, an opioid agonist, and are indicated for the management of pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate. ( 1 ) Limitations of Use ( 1 ) Because of the risks of addiction, abuse, and misuse with opioids, which can occur at any dosage or duration ( 5.2 ) , reserve hydromorphone hydrochloride oral solution or hydromorp…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 87063-039

What is NDC 87063-039?: 87063-039 is the product NDC for Hydromorphone Hydrochloride, Hydromorphone hydrochloride 8 mg/1 tablet, listed with the FDA by ASCLEMED USA INC.. It has 9 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Hydromorphone Hydrochloride.
What is the active ingredient?: Hydromorphone hydrochloride.
Who is the labeler?: ASCLEMED USA INC., NDC labeler code 87063. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Hydromorphone Hydrochloride?: 64 other product NDCs are listed under this name. See all Hydromorphone 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 Hydromorphone Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Hydromorphone Hydrochloride	Hydromorphone hydrochloride 4 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-998	60760-0998-60
Hydromorphone Hydrochloride	Hydromorphone hydrochloride 2 mg/mL	Injection, SolutionIntramuscular, Intravenous, Subcutaneous	Hikma Pharmaceuticals USA Inc.	0641-6254	00641-6254-01
Hydromorphone Hydrochloride	Hydromorphone hydrochloride 1 mg/mL	InjectionIntramuscular, Intravenous, Subcutaneous	Hikma Pharmaceuticals USA Inc.	0641-6169	00641-6169-10
Hydromorphone Hydrochloride	Hydromorphone hydrochloride 2 mg/mL	InjectionIntramuscular, Intravenous, Subcutaneous	Hikma Pharmaceuticals USA Inc.	0641-6170	00641-6170-10
Hydromorphone Hydrochloride	Hydromorphone hydrochloride .5 mg/.5mL	InjectionIntramuscular, Intravenous, Subcutaneous	Hikma Pharmaceuticals USA Inc.	0641-6206	00641-6206-10
Hydromorphone Hydrochloride	Hydromorphone hydrochloride .2 mg/mL	InjectionIntramuscular, Intravenous, Subcutaneous	Hikma Pharmaceuticals USA Inc.	0641-6259	00641-6259-10
Hydromorphone Hydrochloride	Hydromorphone hydrochloride .25 mg/.5mL	Injection, SolutionIntramuscular, Intravenous, Subcutaneous	Hospira, Inc.	0409-1805	00409-1805-01
Hydromorphone Hydrochloride	Hydromorphone hydrochloride .5 mg/.5mL	Injection, SolutionIntramuscular, Intravenous, Subcutaneous	Hospira, Inc.	0409-4264	00409-4264-01
Hydromorphone Hydrochloride	Hydromorphone hydrochloride 5 mg/5mL	SolutionOral	American Health Packaging	60687-566	60687-0566-86
Hydromorphone Hydrochloride	Hydromorphone hydrochloride 2 mg/1	TabletOral	American Health Packaging	60687-579	60687-0579-01

All 65 Hydromorphone Hydrochloride NDCs

Other NDCs under NDA 019892

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

FDA NDC Directory listings under NDA 019892
Product	Strength	Form · route	Labeler	Product NDC
Hydromorphone Hydrochloride	Hydromorphone hydrochloride 4 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-998
Hydromorphone Hydrochloride	Hydromorphone hydrochloride 2 mg/1	TabletOral	ASCLEMED USA INC.	87063-037
Hydromorphone Hydrochloride	Hydromorphone hydrochloride 4 mg/1	TabletOral	ASCLEMED USA INC.	87063-038
Hydromorphone Hydrochloride	Hydromorphone hydrochloride 4 mg/1	TabletOral	Bryant Ranch Prepack	71335-9701
Hydromorphone Hydrochloride	Hydromorphone hydrochloride 2 mg/1	TabletOral	Bryant Ranch Prepack	63629-4284
Dilaudidhydromorphone hydrochloride	Hydromorphone hydrochloride 2 mg/1	TabletOral	Rhodes Pharmaceuticals LLC	42858-122
Dilaudidhydromorphone hydrochloride	Hydromorphone hydrochloride 4 mg/1	TabletOral	Rhodes Pharmaceuticals LLC	42858-234
Hydromorphone Hydrochloride	Hydromorphone hydrochloride 8 mg/1	TabletOral	Rhodes Pharmaceuticals LLC	42858-303
Hydromorphone Hydrochloride	Hydromorphone hydrochloride 2 mg/1	TabletOral	Rhodes Pharmaceuticals LLC	42858-301
Hydromorphone Hydrochloride	Hydromorphone hydrochloride 4 mg/1	TabletOral	Rhodes Pharmaceuticals LLC	42858-302
Dilaudidhydromorphone hydrochloride	Hydromorphone hydrochloride 8 mg/1	TabletOral	Rhodes Pharmaceuticals LLC	42858-338