What is NDC 62332-075?

62332-075 is the product NDC for Memantine Hydrochloride, Memantine hydrochloride 5 mg/1 tablet, coated, listed with the FDA by Alembic Pharmaceuticals Inc.. It has 7 package NDCs, shown above in 10- and 11-digit form.

Alembic Pharmaceuticals Inc., NDC labeler code 62332. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Memantine Hydrochloride?

111 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Memantine Hydrochloride NDC 62332-075

NDC codes

FDA NDC Directory

Product NDC (as listed)62332-075Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62332-0075Add 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
62332-075-10	6233200751062332007510	100 TABLET, COATED in 1 CARTON (62332-075-10)Marketed from Oct 13, 2015
62332-075-20	6233200752062332007520	20 TABLET, COATED in 1 BOTTLE (62332-075-20)Marketed from Oct 13, 2015
62332-075-30	6233200753062332007530	30 TABLET, COATED in 1 BOTTLE (62332-075-30)Marketed from Oct 13, 2015
62332-075-31	6233200753162332007531	100 TABLET, COATED in 1 BOTTLE (62332-075-31)Marketed from Oct 13, 2015
62332-075-42	6233200754262332007542	3000 TABLET, COATED in 1 BOTTLE (62332-075-42)Marketed from Oct 13, 2015
62332-075-60	6233200756062332007560	60 TABLET, COATED in 1 BOTTLE (62332-075-60)Marketed from Oct 13, 2015
62332-075-91	6233200759162332007591	1000 TABLET, COATED in 1 BOTTLE (62332-075-91)Marketed from Oct 13, 2015

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): Memantine Hydrochloride
Generic name (nonproprietary): memantine hydrochloride
Active ingredients: Memantine hydrochloride — 5 mg/1
Dosage form: Tablet, Coated
Route: Oral
Labeler: Alembic Pharmaceuticals Inc.NDC labeler code 62332
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 200891
Marketing start: Oct 13, 2015
Listing expires: Dec 31, 2027
Other FDA classes: NMDA Receptor Antagonists (Mechanism)
Identifiers: Product ID 62332-075_9792a0a6-a48e-4998-9f5a-c9eaa144edeaSPL ID 9792a0a6-a48e-4998-9f5a-c9eaa144edeaSPL set ID af2b73da-1be4-4b7f-929b-acb3b9a10f78RxCUI 996561, 996571UNII JY0WD0UA60
Pharmacologic class: N-methyl-D-aspartate Receptor Antagonist

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

N462332007510 followed by a unit qualifier and the quantity

Package 62332-0075-10. 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 Oct 11, 2021.

Indications (excerpt from the label)

Memantine hydrochloride is indiacted for the treatment of moderate to severe dementia of the Alzheimer's type. Memantine hydrochloride is an N-methyl-D-aspartate (NMDA)receptor antagonist indicated for the treatment of moderate to severe dementia of the Alzheimer's type

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62332-075

What is NDC 62332-075?: 62332-075 is the product NDC for Memantine Hydrochloride, Memantine hydrochloride 5 mg/1 tablet, coated, listed with the FDA by Alembic Pharmaceuticals Inc.. It has 7 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Memantine Hydrochloride.
What is the active ingredient?: Memantine hydrochloride.
Who is the labeler?: Alembic Pharmaceuticals Inc., NDC labeler code 62332. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Memantine Hydrochloride?: 111 other product NDCs are listed under this name. See all Memantine Hydrochloride 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 Memantine Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Memantine hydrochloride	Memantine hydrochloride 7 mg/1	Capsule, Extended releaseOral	Macleods Pharmaceuticals Limited	33342-219	33342-0219-0733342-0219-12
Memantine hydrochloride	Memantine hydrochloride 14 mg/1	Capsule, Extended releaseOral	Macleods Pharmaceuticals Limited	33342-220	33342-0220-0733342-0220-12
Memantine hydrochloride	Memantine hydrochloride 21 mg/1	Capsule, Extended releaseOral	Macleods Pharmaceuticals Limited	33342-221	33342-0221-0733342-0221-12
Memantine hydrochloride	Memantine hydrochloride 28 mg/1	Capsule, Extended releaseOral	Macleods Pharmaceuticals Limited	33342-222	33342-0222-0733342-0222-12
Memantine Hydrochloride	Memantine hydrochloride 5 mg/1	Tablet, Film coatedOral	Carlsbad Technology, Inc.	61442-192	61442-0192-0561442-0192-60
Memantine Hydrochloride	Memantine hydrochloride 10 mg/1	Tablet, Film coatedOral	Carlsbad Technology, Inc.	61442-193	61442-0193-0561442-0193-60
Memantine Hydrochloridememantine	Memantine hydrochloride 7 mg/1	Capsule, Extended releaseOral	Rising Pharma Holdings, Inc.	16571-852	16571-0852-03
Memantine Hydrochloridememantine	Memantine hydrochloride 14 mg/1	Capsule, Extended releaseOral	Rising Pharma Holdings, Inc.	16571-853	16571-0853-0316571-0853-09
Memantine Hydrochloridememantine	Memantine hydrochloride 21 mg/1	Capsule, Extended releaseOral	Rising Pharma Holdings, Inc.	16571-854	16571-0854-03
Memantine Hydrochloridememantine	Memantine hydrochloride 28 mg/1	Capsule, Extended releaseOral	Rising Pharma Holdings, Inc.	16571-855	16571-0855-0316571-0855-09

All 112 Memantine Hydrochloride NDCs

Other NDCs under ANDA 200891

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

FDA NDC Directory listings under ANDA 200891
Product	Strength	Form · route	Labeler	Product NDC
Memantine Hydrochloride	Memantine hydrochloride 5 mg/1	Tablet, CoatedOral	Alembic Pharmaceuticals Limited	46708-451
Memantine Hydrochloride	Memantine hydrochloride 10 mg/1	Tablet, CoatedOral	Alembic Pharmaceuticals Limited	46708-452
Memantine Hydrochloride	Memantine hydrochloride 10 mg/1	Tablet, CoatedOral	Alembic Pharmaceuticals Inc.	62332-076