Drug
Who makes memantine hydrochloride?
33 companies list memantine hydrochloride as a human prescription drug. Forms: capsule, extended release; kit; solution; tablet; tablet, coated; tablet, film coated. Routes: oral.
Labellers from the openFDA NDC Directory. A labeller is the firm named on the label, not necessarily the site that made the product, and a listing is not an FDA approval. Data as of 24 Sept 2026. Methodology
Companies listing memantine hydrochloride
| Company | Forms | Application | NDCs | Registered sites |
|---|---|---|---|---|
| Bryant Ranch PrepackUnited States | tablet; tablet, film coated | ANDAANDA090058, ANDA090961, ANDA206528 | 11 | 1 |
| Aurobindo Pharma LimitedIndia | capsule, extended release; kit; tablet, film coated | ANDAANDA203175, ANDA214651 | 7 | 6 |
| Macleods Pharmaceuticals LimitedIndia | capsule, extended release; solution; tablet | ANDAANDA202790, ANDA202840, ANDA206310 | 7 | 5 |
| International Medication Systems, Ltd.United States | tablet; tablet, film coated | ANDAANDA090961, ANDA200022, ANDA202840 | 7 | 3 |
| Lupin LimitedIndia | capsule, extended release; tablet, film coated | ANDAANDA090051, ANDA206028 | 6 | 14 |
| Zydus Lifesciences LimitedIndia | capsule, extended release; tablet, film coated | ANDAANDA090961, ANDA203293 | 6 | 12 |
| Cardinal Health 418, Inc.United States | tablet; tablet, film coated | ANDA, NDA AUTHORIZED GENERICANDA090048, NDA021487 | 4 | 34 |
| Alembic Pharmaceuticals LimitedIndia | tablet, coated | ANDAANDA200891 | 4 | 7 |
| Amneal Ireland LimitedIreland | capsule, extended release | ANDAANDA205825 | 4 | 1 |
| Slate Run Pharmaceuticals, LLCUnited States | capsule, extended release | ANDAANDA211100 | 4 | 1 |
| Zydus Pharmaceuticals USA Inc.India | capsule, extended release | ANDAANDA203293 | 4 | 1 |
| Aphena Pharma Solutions - Tennessee, LLC | tablet; tablet, film coated | ANDA, NDAANDA090961, ANDA200022, ANDA206528 | 4 | 0 |
| MAJOR Pharmaceuticals Inc. | capsule, extended release; tablet, film coated | ANDAANDA090048, ANDA206028 | 4 | 0 |
| Vitruvias Therapeutics, Inc. | capsule, extended release | ANDAANDA213985 | 4 | 0 |
| Actavis LLCUnited States | kit; tablet | NDA AUTHORIZED GENERICNDA021487 | 3 | 1 |
| Sun Pharmaceutical Industries LimitedIndia | tablet, film coated | ANDAANDA090058 | 2 | 13 |
| Unichem Laboratories Limited, IndiaIndia | tablet, film coated | ANDAANDA200022 | 2 | 5 |
| Ajanta Pharma LimitedIndia | tablet | ANDAANDA206528 | 2 | 2 |
| Camber Pharmaceuticals, Inc.United States | tablet | ANDAANDA204389 | 2 | 1 |
| Carlsbad Technology, Inc.United States | tablet, film coated | ANDAANDA212947 | 2 | 1 |
| POLYGEN PHARMACEUTICALS INC.United States | tablet, film coated | ANDAANDA210587 | 2 | 1 |
| AvPAK | tablet, film coated | ANDAANDA200022 | 2 | 0 |
| Dr. Reddys Laboratories Limited | tablet, film coated | ANDAANDA090048 | 2 | 0 |
| Upsher-Smith Laboratories, Inc. | tablet, film coated | ANDAANDA090043 | 2 | 0 |
| Viona Pharmaceuticals Inc. | tablet | ANDAANDA090961 | 2 | 0 |
| Apotex Inc.Canada | solution | ANDAANDA209955 | 1 | 6 |
| Coupler LLCUnited States | tablet | ANDAANDA090961 | 1 | 1 |
| NCS HealthCare of KY, LLC dba Vangard LabsUnited States | capsule, extended release | ANDAANDA214651 | 1 | 1 |
| Preferred Pharmaceuticals Inc.United States | tablet | ANDAANDA206528 | 1 | 1 |
| RemedyRepack, IncUnited States | tablet | ANDAANDA090961 | 1 | 1 |
| Chartwell Governmental & Specialty RX, LLC. | solution | ANDAANDA204033 | 1 | 0 |
| Chartwell RX, LLC. | solution | ANDAANDA204033 | 1 | 0 |
| DirectRx | tablet | ANDAANDA090961 | 1 | 0 |
Bulk ingredient listings
- Chemo Biosynthesis s.r.l.Italy · 4 NDC
- Industriale Chimica SRLItaly · 3 NDC
- PROCOS SpAItaly · 2 NDC
- Anonima Materie Sintetiche and Affini (AMSA) SpA · 1 NDC
- Apotex Inc.Canada · 1 NDC
- Cohance Lifesciences LimitedIndia · 1 NDC
- Dr. Reddy's Laboratories LimitedIndia · 1 NDC
- Emcure Pharmaceuticals LimitedIndia · 1 NDC
- Hainan Poly Pharm. Co., Ltd.China · 1 NDC
- Hetero Drugs LimitedIndia · 1 NDC
- Hikal LimitedIndia · 1 NDC
- MSN Pharmachem Private LimitedIndia · 1 NDC
- Megafine Pharma (P) LimitedIndia · 1 NDC
- Olon USA LLCItaly · 1 NDC
- Olpha ASLatvia · 1 NDC
- Optimus Drugs Private LimitedIndia · 1 NDC
- Siegfried Evionnaz SA · 1 NDC
- Unichem Laboratories Limited, IndiaIndia · 1 NDC
- Uquifa Spain · 1 NDC
- WanYang Hengshui Pharmaceutical Co LtdChina · 1 NDC
Orange Book patents
2 unexpired patents list memantine hydrochloride as the active ingredient, expiring between Mar 2029 and Sept 2029. Application holder: ABBVIE INC.
Enquiry
Common questions
- Who makes memantine hydrochloride?
- 33 companies list memantine hydrochloride as a human prescription drug in the openFDA NDC Directory, led by Bryant Ranch Prepack, Aurobindo Pharma Limited, Macleods Pharmaceuticals Limited, International Medication Systems, Ltd., Lupin Limited. Each is the labeller, the firm named on the label; the product may be made at a site registered to another company.
- Is there a generic memantine hydrochloride?
- 32 companies list memantine hydrochloride under an abbreviated new drug application (ANDA), the application type used for generics, and 1 under an NDA or BLA. Listing status is from the NDC Directory; it is not a statement of availability.
- Who supplies memantine hydrochloride active ingredient?
- 20 companies list memantine hydrochloride as a bulk ingredient, including Chemo Biosynthesis s.r.l., Industriale Chimica SRL, PROCOS SpA, Anonima Materie Sintetiche and Affini (AMSA) SpA.