What is NDC 50090-5926?

50090-5926 is the product NDC for Memantine Hydrochloride, Memantine hydrochloride 5 mg/1 tablet, film coated, listed with the FDA by A-S Medication Solutions. It has 2 package NDCs, shown above in 10- and 11-digit form.

A-S Medication Solutions, NDC labeler code 50090. 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 50090-5926

NDC codes

FDA NDC Directory

Product NDC (as listed)50090-5926Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50090-5926Add 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	Copy
50090-5926-0	5009059260050090592600	60 TABLET, FILM COATED in 1 BOTTLE (50090-5926-0)Marketed from Mar 1, 2022
50090-5926-1	5009059260150090592601	90 TABLET, FILM COATED in 1 BOTTLE (50090-5926-1)Marketed from Jul 2, 2022

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): Memantine Hydrochloride
Generic name (nonproprietary): memantine hydrochloride
Active ingredients: Memantine hydrochloride — 5 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: A-S Medication SolutionsNDC labeler code 50090
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 200022
Marketing start: Nov 1, 2015
Listing expires: Dec 31, 2026
Other FDA classes: NMDA Receptor Antagonists (Mechanism)
Identifiers: Product ID 50090-5926_99e7c450-2c83-487e-a326-76c1653723b8SPL ID 99e7c450-2c83-487e-a326-76c1653723b8SPL set ID 2fdf0b2b-0337-472d-83ec-075c17c9b0d0RxCUI 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

N450090592600 followed by a unit qualifier and the quantity

Package 50090-5926-00. 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 Nov 22, 2023.

Indications (excerpt from the label)

Memantine hydrochloride tablets are an N-methyl-D-asparate (NMDA) receptor antagonist indicated for the treatment of moderate to severe dementia of the Alzheimer's type. ( 1 ) Memantine hydrochloride tablets are 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 50090-5926

What is NDC 50090-5926?: 50090-5926 is the product NDC for Memantine Hydrochloride, Memantine hydrochloride 5 mg/1 tablet, film coated, listed with the FDA by A-S Medication Solutions. It has 2 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?: A-S Medication Solutions, NDC labeler code 50090. 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 200022

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

FDA NDC Directory listings under ANDA 200022
Product	Strength	Form · route	Labeler	Product NDC
Memantine Hydrochloride	Memantine hydrochloride 5 mg/1	Tablet, Film coatedOral	Unichem Pharmaceuticals (USA), Inc.	29300-171
Memantine Hydrochloride	Memantine hydrochloride 10 mg/1	Tablet, Film coatedOral	Unichem Pharmaceuticals (USA), Inc.	29300-172
Memantine Hydrochloride	Memantine hydrochloride 10 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-4434
Memantine Hydrochloride	Memantine hydrochloride 5 mg/1	Tablet, Film coatedOral	AvPAK	50268-587
Memantine Hydrochloride	Memantine hydrochloride 10 mg/1	Tablet, Film coatedOral	AvPAK	50268-588
Memantine Hydrochloride	Memantine hydrochloride 5 mg/1	Tablet, Film coatedOral	Aphena Pharma Solutions - Tennessee, LLC	71610-979