Prescription drug · ANDA
Memantine Hydrochloride NDC 70518-3338
Memantine hydrochloride 5 mg/1 · Tablet · Oral · REMEDYREPACK INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70518-3338-2 | 7051833380270518333802 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-3338-2)Marketed from May 28, 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)
- Memantine Hydrochloride
- Generic name (nonproprietary)
- memantine hydrochloride
- Active ingredients
- Memantine hydrochloride — 5 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- REMEDYREPACK INC.NDC labeler code 70518
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 090961
- Marketing start
- Listing expires
- Other FDA classes
- NMDA Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 70518-3338_5864e034-0649-7cc6-e063-6294a90abae0SPL ID 5864e034-0649-7cc6-e063-6294a90abae0SPL set ID cbfd9d95-f50b-45ff-9857-9f1712c45e56RxCUI 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
N470518333802followed by a unit qualifier and the quantityPackage 70518-3338-02. 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)
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. ( 1 ) Memantine hydrochloride tablets, USP are indicated for the treatment of moderate to severe dementia of the Alzheimer's type.
Excerpt only. Read the full label for complete information.
About NDC 70518-3338
- What is NDC 70518-3338?
- 70518-3338 is the product NDC for Memantine Hydrochloride, Memantine hydrochloride 5 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, 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?
- REMEDYREPACK INC., NDC labeler code 70518. 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.
Related NDCs: other Memantine Hydrochloride products
Other finished products listed under the same name: strengths, forms and labelers.
| 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 |
Other NDCs under ANDA 090961
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Memantine Hydrochloride | Memantine hydrochloride 5 mg/1 | TabletOral | A-S Medication Solutions | 50090-6291 |
| Memantine Hydrochloride | Memantine hydrochloride 10 mg/1 | TabletOral | Bryant Ranch Prepack | 63629-2511 |
| Memantine Hydrochloride | Memantine hydrochloride 10 mg/1 | TabletOral | Bryant Ranch Prepack | 63629-2512 |
| Memantine Hydrochloride | Memantine hydrochloride 5 mg/1 | TabletOral | Bryant Ranch Prepack | 63629-2513 |
| Memantine Hydrochloride | Memantine hydrochloride 5 mg/1 | TabletOral | Bryant Ranch Prepack | 63629-2514 |
| Memantine Hydrochloride | Memantine hydrochloride 5 mg/1 | TabletOral | Coupler LLC | 67046-1471 |
| Memantine Hydrochloride | Memantine hydrochloride 5 mg/1 | Tablet, Film coatedOral | Zydus Lifesciences Limited | 70771-1119 |
| Memantine Hydrochloride | Memantine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Zydus Lifesciences Limited | 70771-1120 |
| Memantine Hydrochloride | Memantine hydrochloride 10 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-1603 |
| Memantine Hydrochloride | Memantine hydrochloride 5 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-1732 |
| Memantine Hydrochloride | Memantine hydrochloride 5 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-2013 |
| Memantine Hydrochloride | Memantine hydrochloride 5 mg/1 | TabletOral | Aphena Pharma Solutions - Tennessee, LLC | 71610-911 |
| Memantine Hydrochloride | Memantine hydrochloride 5 mg/1 | TabletOral | Bryant Ranch Prepack | 72162-2003 |
| Memantine Hydrochloride | Memantine hydrochloride 10 mg/1 | TabletOral | Bryant Ranch Prepack | 72162-2004 |
| Memantine Hydrochloride | Memantine hydrochloride 5 mg/1 | TabletOral | DirectRx | 72189-294 |
| Memantine Hydrochloride | Memantine hydrochloride 5 mg/1 | TabletOral | Viona Pharmaceuticals Inc | 72578-003 |
| Memantine Hydrochloride | Memantine hydrochloride 10 mg/1 | TabletOral | Viona Pharmaceuticals Inc | 72578-004 |