NDC codes

FDA NDC Directory
Product NDC (as listed)71335-9662Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-9662Add 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
71335-9662-17133596620160 TABLET in 1 BOTTLE (71335-9662-1)Marketed from Apr 13, 2026
71335-9662-27133596620230 TABLET in 1 BOTTLE (71335-9662-2)Marketed from Apr 13, 2026
71335-9662-37133596620390 TABLET in 1 BOTTLE (71335-9662-3)Marketed from Mar 2, 2023
71335-9662-471335966204120 TABLET in 1 BOTTLE (71335-9662-4)Marketed from Apr 13, 2026
71335-9662-57133596620515 TABLET in 1 BOTTLE (71335-9662-5)Marketed from Apr 13, 2026
71335-9662-671335966206180 TABLET in 1 BOTTLE (71335-9662-6)Marketed from Apr 13, 2026
71335-9662-77133596620720 TABLET in 1 BOTTLE (71335-9662-7)Marketed from Apr 13, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 — 30 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212451
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Full Opioid Agonists (Mechanism)
Identifiers
Product ID 71335-9662_b1e7450b-172b-49ae-8d13-b5a68dbd7656SPL ID b1e7450b-172b-49ae-8d13-b5a68dbd7656SPL set ID d1b0b4ac-69d9-44bf-b7a3-229bd89b9fd6RxCUI 892672UNII 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

N471335966201 followed by a unit qualifier and the quantity

Package 71335-9662-01. 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)

Morphine sulfate tablets are indicated for the management of: adult and pediatric patients weighing at least 50 kg and above with acute pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate. adults with chronic pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate. 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 ( 5.1 )], reserve morphine sulfate tablets for use in patients for whom alternative treatment options (e.g., non-opioid analgesics or opioid combination products): Have not been …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 212451

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

FDA NDC Directory listings under ANDA 212451
ProductStrengthForm · routeLabelerProduct NDC
Morphine SulfateMorphine sulfate 15 mg/1TabletOralBryant Ranch Prepack63629-8459
Morphine SulfateMorphine sulfate 15 mg/1TabletOralAmerican Health Packaging60687-617
Morphine SulfateMorphine sulfate 15 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-893
Morphine SulfateMorphine sulfate 15 mg/1TabletOralAscend Laboratories, LLC67877-670
Morphine SulfateMorphine sulfate 30 mg/1TabletOralAscend Laboratories, LLC67877-671

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