Prescription drug · NDA AUTHORIZED GENERIC

Hydromorphone Hydrochloride NDC 87063-037

Hydromorphone hydrochloride 2 mg/1 · Tablet · Oral · ASCLEMED USA INC.

NDC codes

FDA NDC Directory
Product NDC (as listed)87063-037Labeler and product segments. Claims need a package NDC.
Product NDC at billing width87063-0037Add 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
87063-037-0187063003701100 TABLET in 1 BOTTLE, PLASTIC (87063-037-01)Marketed from Dec 4, 2025
87063-037-05870630037055 TABLET in 1 BOTTLE, PLASTIC (87063-037-05)Marketed from Dec 4, 2025
87063-037-07870630037077 TABLET in 1 BOTTLE, PLASTIC (87063-037-07)Marketed from Dec 4, 2025
87063-037-108706300371010 TABLET in 1 BOTTLE, PLASTIC (87063-037-10)Marketed from Dec 4, 2025
87063-037-148706300371414 TABLET in 1 BOTTLE, PLASTIC (87063-037-14)Marketed from Dec 4, 2025
87063-037-208706300372020 TABLET in 1 BOTTLE, PLASTIC (87063-037-20)Marketed from Dec 4, 2025
87063-037-308706300373030 TABLET in 1 BOTTLE, PLASTIC (87063-037-30)Marketed from Dec 4, 2025
87063-037-608706300376060 TABLET in 1 BOTTLE, PLASTIC (87063-037-60)Marketed from Dec 4, 2025
87063-037-908706300379090 TABLET in 1 BOTTLE, PLASTIC (87063-037-90)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 — 2 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
NDA authorized genericApplication NDA 019892
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Full Opioid Agonists (Mechanism)
Identifiers
Product ID 87063-037_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

N487063003701 followed by a unit qualifier and the quantity

Package 87063-0037-01. 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)

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)

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
ProductStrengthForm · routeLabelerProduct NDC
Hydromorphone HydrochlorideHydromorphone hydrochloride 2 mg/1TabletOralBryant Ranch Prepack63629-4284
Hydromorphone HydrochlorideHydromorphone hydrochloride 4 mg/1TabletOralASCLEMED USA INC.87063-038
Hydromorphone HydrochlorideHydromorphone hydrochloride 8 mg/1TabletOralASCLEMED USA INC.87063-039
Dilaudidhydromorphone hydrochlorideHydromorphone hydrochloride 2 mg/1TabletOralRhodes Pharmaceuticals LLC42858-122
Hydromorphone HydrochlorideHydromorphone hydrochloride 4 mg/1TabletOralBryant Ranch Prepack71335-9701
Hydromorphone HydrochlorideHydromorphone hydrochloride 2 mg/1TabletOralRhodes Pharmaceuticals LLC42858-301
Dilaudidhydromorphone hydrochlorideHydromorphone hydrochloride 4 mg/1TabletOralRhodes Pharmaceuticals LLC42858-234
Hydromorphone HydrochlorideHydromorphone hydrochloride 4 mg/1TabletOralRhodes Pharmaceuticals LLC42858-302
Hydromorphone HydrochlorideHydromorphone hydrochloride 8 mg/1TabletOralRhodes Pharmaceuticals LLC42858-303
Dilaudidhydromorphone hydrochlorideHydromorphone hydrochloride 8 mg/1TabletOralRhodes Pharmaceuticals LLC42858-338
Hydromorphone HydrochlorideHydromorphone hydrochloride 4 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-998

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Hydromorphone Hydrochloride NDC 87063-037 | Med-Code