NDC codes

FDA NDC Directory
Product NDC (as listed)63629-2364Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63629-2364Add 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
63629-2364-16362923640130 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2364-1)Marketed from Feb 9, 2011

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)
Galantamine Hydrobromide
Generic name (nonproprietary)
galantamine hydrobromide
Active ingredients
Galantamine hydrobromide — 8 mg/1
Dosage form
Capsule, Extended release
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 63629
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090178
Marketing start
Listing expires
Other FDA classes
Cholinesterase Inhibitors (Mechanism)
Identifiers
Product ID 63629-2364_241d4ec3-7582-4846-8d78-6b9840053c98SPL ID 241d4ec3-7582-4846-8d78-6b9840053c98SPL set ID db5b6c1e-449b-413f-b0cc-ca2133aa4986RxCUI 860715UNII MJ4PTD2VVW
Pharmacologic class
Cholinesterase Inhibitor

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

N463629236401 followed by a unit qualifier and the quantity

Package 63629-2364-01. 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 .

Indications (excerpt from the label)

Galantamine hydrobromide extended-release capsules are indicated for the treatment of mild to moderate dementia of the Alzheimer's type. Galantamine hydrobromide is a cholinesterase inhibitor indicated for the treatment of mild to moderate dementia of the Alzheimer’s type ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63629-2364

What is NDC 63629-2364?
63629-2364 is the product NDC for Galantamine Hydrobromide, Galantamine hydrobromide 8 mg/1 capsule, extended release, 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?
Galantamine Hydrobromide.
What is the active ingredient?
Galantamine hydrobromide.
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 Galantamine Hydrobromide?
9 other product NDCs are listed under this name. See all Galantamine Hydrobromide 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 Galantamine Hydrobromide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Galantamine HydrobromideGalantamine hydrobromide 8 mg/1Capsule, Extended releaseOralSun Pharmaceutical Industries, Inc.47335-83547335-0835-0847335-0835-1847335-0835-83+1 more
Galantamine HydrobromideGalantamine hydrobromide 16 mg/1Capsule, Extended releaseOralSun Pharmaceutical Industries, Inc.47335-83647335-0836-0847335-0836-1847335-0836-83+1 more
Galantamine HydrobromideGalantamine hydrobromide 24 mg/1Capsule, Extended releaseOralSun Pharmaceutical Industries, Inc.47335-83747335-0837-0847335-0837-1847335-0837-83+1 more
Galantamine HydrobromideGalantamine hydrobromide 24 mg/1Capsule, Extended releaseOralBryant Ranch Prepack63629-236363629-2363-01
Galantamine HydrobromideGalantamine hydrobromide 16 mg/1Capsule, Extended releaseOralBryant Ranch Prepack63629-236563629-2365-01
Galantamine HydrobromideGalantamine hydrobromide 8 mg/1Capsule, Extended releaseOralBryant Ranch Prepack72162-144672162-1446-03
Galantamine HydrobromideGalantamine hydrobromide 16 mg/1Capsule, Extended releaseOralBryant Ranch Prepack72162-144772162-1447-03
Galantamine HydrobromideGalantamine hydrobromide 24 mg/1Capsule, Extended releaseOralBryant Ranch Prepack72162-144872162-1448-03
Galantamine HydrobromideGalantamine hydrobromide 4 mg/mLSolutionOralHikma Pharmaceuticals USA Inc.0054-013700054-0137-49

Other NDCs under ANDA 090178

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

FDA NDC Directory listings under ANDA 090178
ProductStrengthForm · routeLabelerProduct NDC
Galantamine HydrobromideGalantamine hydrobromide 8 mg/1Capsule, Extended releaseOralSun Pharmaceutical Industries, Inc.47335-835
Galantamine HydrobromideGalantamine hydrobromide 16 mg/1Capsule, Extended releaseOralSun Pharmaceutical Industries, Inc.47335-836
Galantamine HydrobromideGalantamine hydrobromide 24 mg/1Capsule, Extended releaseOralSun Pharmaceutical Industries, Inc.47335-837
Galantamine HydrobromideGalantamine hydrobromide 24 mg/1Capsule, Extended releaseOralBryant Ranch Prepack63629-2363
Galantamine HydrobromideGalantamine hydrobromide 16 mg/1Capsule, Extended releaseOralBryant Ranch Prepack63629-2365
Galantamine HydrobromideGalantamine hydrobromide 8 mg/1Capsule, Extended releaseOralBryant Ranch Prepack72162-1446
Galantamine HydrobromideGalantamine hydrobromide 16 mg/1Capsule, Extended releaseOralBryant Ranch Prepack72162-1447
Galantamine HydrobromideGalantamine hydrobromide 24 mg/1Capsule, Extended releaseOralBryant Ranch Prepack72162-1448

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