NDC codes

FDA NDC Directory
Product NDC (as listed)68094-045Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68094-0045Add 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
68094-045-586809400455850 BAG in 1 CASE (68094-045-58) / 1 SYRINGE in 1 BAG / .5 mL in 1 SYRINGE (68094-045-01)Marketed from Nov 1, 2020

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 — 100 mg/5mL
Dosage form
Solution
Route
Oral
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 022195
Marketing start
Marketing end
DEA schedule
CII
Other FDA classes
Full Opioid Agonists (Mechanism)
Identifiers
Product ID 68094-045_2e5222a7-582a-44cf-aedd-53c6b7f99edaSPL ID 2e5222a7-582a-44cf-aedd-53c6b7f99edaSPL set ID 67f0ee8d-696e-4c08-9007-3df0e3988badRxCUI 892625UNII 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

N468094004558 followed by a unit qualifier and the quantity

Package 68094-0045-58. 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)

Morphine Sulfate Oral Solution 2 mg/mL and 4 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. pediatric patients 2 years of age and older with acute 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…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 022195

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

FDA NDC Directory listings under NDA 022195
ProductStrengthForm · routeLabelerProduct NDC
Morphine SulfateMorphine sulfate 20 mg/5mLSolutionOralHikma Pharmaceuticals USA Inc.0054-0238
Morphine SulfateMorphine sulfate 10 mg/5mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-0904
Morphine SulfateMorphine sulfate 100 mg/5mLSolutionOralHikma Pharmaceuticals USA Inc.0054-0517
Morphine SulfateMorphine sulfate 10 mg/5mLSolutionOralPrecision Dose Inc.68094-001
Morphine SulfateMorphine sulfate 10 mg/5mLSolutionOralHikma Pharmaceuticals USA Inc.0054-0237
Morphine SulfateMorphine sulfate 100 mg/5mLSolutionOralPrecision Dose, Inc.68094-056
Morphine SulfateMorphine sulfate 10 mg/5mLSolutionOralAmerican Health Packaging60687-760
Morphine SulfateMorphine sulfate 100 mg/5mLSolutionOralPrecision Dose, Inc.68094-156
Morphine SulfateMorphine sulfate 100 mg/5mLSolutionOralPrecision Dose, Inc.68094-356
Morphine SulfateMorphine sulfate 100 mg/5mLSolutionOralPrecision Dose, Inc.68094-556

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