What is NDC 60687-927?

60687-927 is the product NDC for Morphine Sulfate, Morphine sulfate 10 mg/5mL solution, listed with the FDA by American Health Packaging. It has 1 package NDC, shown above in 10- and 11-digit form.

American Health Packaging, NDC labeler code 60687. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Morphine Sulfate?

126 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Morphine Sulfate NDC 60687-927 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)60687-927Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60687-0927Add 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
60687-927-86	6068709278660687092786	3 TRAY in 1 CASE (60687-927-86) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-927-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-927-40)Marketed from Feb 1, 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): Morphine Sulfate
Generic name (nonproprietary): morphine sulfate
Active ingredients: Morphine sulfate — 10 mg/5mL
Dosage form: Solution
Route: Oral
Labeler: American Health PackagingNDC labeler code 60687
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 206573
Marketing start: Feb 1, 2026
Listing expires: Dec 31, 2027
DEA schedule: CII
Other FDA classes: Full Opioid Agonists (Mechanism)
Identifiers: Product ID 60687-927_4a17fffd-a5d3-d770-e063-6294a90ace0cSPL ID 4a17fffd-a5d3-d770-e063-6294a90ace0cSPL set ID 66a3f607-7f48-490f-84dd-b74dd1ee39e5RxCUI 892589UNII X3P646A2J0
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

N460687092786 followed by a unit qualifier and the quantity

Package 60687-0927-86. 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 Feb 5, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Morphine Sulfate Oral Solution 2 mg/mL is indicated for the management of: adults with acute and chronic pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate. Morphine Sulfate Oral Solution 20 mg/mL is indicated for the relief of acute and chronic pain in opioid-tolerant adult patients. Limitations of Use Because of the risks of addiction, abuse, and misuse with opioids, which can occur at any dosage or duration [see Warnings and Precautions (5.2) ] , reserve Morphine Sulfate Oral Solution for use in patients for whom alternative treatment options (e.g., non-opioid analgesics or opioid combination products): Have not been tolerated, or are not…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60687-927

What is NDC 60687-927?: 60687-927 is the product NDC for Morphine Sulfate, Morphine sulfate 10 mg/5mL solution, listed with the FDA by American Health Packaging. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Morphine Sulfate.
What is the active ingredient?: Morphine sulfate.
Who is the labeler?: American Health Packaging, NDC labeler code 60687. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Morphine Sulfate?: 126 other product NDCs are listed under this name. See all Morphine Sulfate 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 Morphine Sulfate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Morphine Sulfate	Morphine sulfate 15 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-893	60760-0893-60
Morphine Sulfate	Morphine sulfate 20 mg/mL	SolutionOral	American Health Packaging	68000-110	68000-0110-01
Morphine Sulfate	Morphine sulfate 20 mg/mL	SolutionOral	American Health Packaging	68000-111	68000-0111-05
Morphine Sulfate	Morphine sulfate 20 mg/mL	SolutionOral	American Health Packaging	68000-112	68000-0112-05
Morphine Sulfate	Morphine sulfate 20 mg/mL	SolutionOral	American Health Packaging	68000-113	68000-0113-03
Morphine Sulfate	Morphine sulfate 20 mg/mL	SolutionOral	American Health Packaging	68000-114	68000-0114-03
Morphine Sulfate	Morphine sulfate 10 mg/5mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-4955	00121-4955-94
Morphine Sulfate	Morphine sulfate 100 mg/5mL	SolutionOral	Precision Dose, Inc.	68094-556	68094-0556-58
Morphine Sulfate	Morphine sulfate 100 mg/5mL	SolutionOral	Precision Dose, Inc.	68094-156	68094-0156-58
Morphine sulfate	Morphine sulfate 50 mg/mL	Injection, SolutionIntravenous	Hospira, Inc.	0409-2022	00409-2022-01

All 127 Morphine Sulfate NDCs

Other NDCs under ANDA 206573

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

FDA NDC Directory listings under ANDA 206573
Product	Strength	Form · route	Labeler	Product NDC
Morphine Sulfate	Morphine sulfate 10 mg/5mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-4955