What is NDC 71335-9662?

71335-9662 is the product NDC for Morphine Sulfate, Morphine sulfate 30 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 7 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. 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 71335-9662 | National Drug Code

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 NDC	11-digit (billing)	Package
71335-9662-1	7133596620171335966201	60 TABLET in 1 BOTTLE (71335-9662-1)Marketed from Apr 13, 2026
71335-9662-2	7133596620271335966202	30 TABLET in 1 BOTTLE (71335-9662-2)Marketed from Apr 13, 2026
71335-9662-3	7133596620371335966203	90 TABLET in 1 BOTTLE (71335-9662-3)Marketed from Mar 2, 2023
71335-9662-4	7133596620471335966204	120 TABLET in 1 BOTTLE (71335-9662-4)Marketed from Apr 13, 2026
71335-9662-5	7133596620571335966205	15 TABLET in 1 BOTTLE (71335-9662-5)Marketed from Apr 13, 2026
71335-9662-6	7133596620671335966206	180 TABLET in 1 BOTTLE (71335-9662-6)Marketed from Apr 13, 2026
71335-9662-7	7133596620771335966207	20 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
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 212451
Marketing start: Feb 11, 2021
Listing expires: Dec 31, 2027
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 Apr 13, 2026. 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)

About NDC 71335-9662

What is NDC 71335-9662?: 71335-9662 is the product NDC for Morphine Sulfate, Morphine sulfate 30 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 7 package NDCs, 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?: Bryant Ranch Prepack, NDC labeler code 71335. 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	American Health Packaging	60687-927	60687-0927-86
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

All 127 Morphine Sulfate NDCs

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
Product	Strength	Form · route	Labeler	Product NDC
Morphine Sulfate	Morphine sulfate 15 mg/1	TabletOral	American Health Packaging	60687-617
Morphine Sulfate	Morphine sulfate 15 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-893
Morphine Sulfate	Morphine sulfate 15 mg/1	TabletOral	Bryant Ranch Prepack	63629-8459
Morphine Sulfate	Morphine sulfate 15 mg/1	TabletOral	Ascend Laboratories, LLC	67877-670
Morphine Sulfate	Morphine sulfate 30 mg/1	TabletOral	Ascend Laboratories, LLC	67877-671