NDC codes

FDA NDC Directory
Product NDC (as listed)63629-8459Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63629-8459Add 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
63629-8459-16362984590163629845901100 TABLET in 1 BOTTLE (63629-8459-1)Marketed from Jun 16, 2025

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 — 15 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 63629
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 63629-8459_905cd842-2c86-4318-a6c4-92f49de145b3SPL ID 905cd842-2c86-4318-a6c4-92f49de145b3SPL set ID 905cd842-2c86-4318-a6c4-92f49de145b3RxCUI 892582UNII 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

N463629845901 followed by a unit qualifier and the quantity

Package 63629-8459-01. 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)

About NDC 63629-8459

What is NDC 63629-8459?
63629-8459 is the product NDC for Morphine Sulfate, Morphine sulfate 15 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. 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?
Bryant Ranch Prepack, NDC labeler code 63629. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Morphine SulfateMorphine sulfate 15 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-89360760-0893-60
Morphine SulfateMorphine sulfate 20 mg/mLSolutionOralAmerican Health Packaging68000-11068000-0110-01
Morphine SulfateMorphine sulfate 20 mg/mLSolutionOralAmerican Health Packaging68000-11168000-0111-05
Morphine SulfateMorphine sulfate 20 mg/mLSolutionOralAmerican Health Packaging68000-11268000-0112-05
Morphine SulfateMorphine sulfate 20 mg/mLSolutionOralAmerican Health Packaging68000-11368000-0113-03
Morphine SulfateMorphine sulfate 20 mg/mLSolutionOralAmerican Health Packaging68000-11468000-0114-03
Morphine SulfateMorphine sulfate 10 mg/5mLSolutionOralAmerican Health Packaging60687-92760687-0927-86
Morphine SulfateMorphine sulfate 10 mg/5mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-495500121-4955-94
Morphine SulfateMorphine sulfate 100 mg/5mLSolutionOralPrecision Dose, Inc.68094-55668094-0556-58
Morphine SulfateMorphine sulfate 100 mg/5mLSolutionOralPrecision Dose, Inc.68094-15668094-0156-58

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
ProductStrengthForm · routeLabelerProduct NDC
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
Morphine SulfateMorphine sulfate 30 mg/1TabletOralBryant Ranch Prepack71335-9662

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