65862-652 : Memantine Hydrochloride 5 mg Oral Tablet, Film Coated
NDC: | 65862-652 |
Labeler: | Aurobindo Pharma Limited |
Product Type: | Human Prescription Drug |
Drug Name: | Memantine Hydrochloride |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA203175 |
Rev. Date: |
Appearance:
Markings: | Z;01 |
Shapes: |
Capsule |
Colors: |
White |
Size (mm): | 10 |
Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. |
NDC Package Codes:
- 65862-652-03: 3 BLISTER PACK IN 1 CARTON (65862‑652‑03) > 10 TABLET, FILM COATED IN 1 BLISTER PACK (65862‑652‑10)
- 65862-652-60: 60 TABLET, FILM COATED IN 1 BOTTLE (65862‑652‑60)
- 65862-652-78: 10 BLISTER PACK IN 1 CARTON (65862‑652‑78) > 10 TABLET, FILM COATED IN 1 BLISTER PACK (65862‑652‑10)
- 65862-652-99: 1000 TABLET, FILM COATED IN 1 BOTTLE (65862‑652‑99)
Active Ingredients:
- Memantine Hydrochloride
Dosage Strength:
- 5 mg
Inactive Ingredients:
- Silicon Dioxide
- Hydroxypropyl Cellulose (Type H)
- Cellulose, Microcrystalline
- Polyethylene Glycol 6000
- Sodium Starch Glycolate Type a Potato
- Sodium Stearyl Fumarate
- Talc
- Titanium Dioxide
Pharmaceutical Classes:
- NMDA Receptor Antagonists [MoA]
- N-methyl-D-aspartate Receptor Antagonist [EPC]
Related Products:
Based on records with the same trade name.- 65862-653 Memantine Hydrochloride 10 mg Oral Tablet, Film Coated by Aurobindo Pharma Limited
- 59651-404 Memantine Hydrochloride 7 mg Oral Capsule, Extended Release by Aurobindo Pharma Limited
- 59651-405 Memantine Hydrochloride 14 mg Oral Capsule, Extended Release by Aurobindo Pharma Limited
- 59651-406 Memantine Hydrochloride 21 mg Oral Capsule, Extended Release by Aurobindo Pharma Limited
- 59651-407 Memantine Hydrochloride 28 mg Oral Capsule, Extended Release by Aurobindo Pharma Limited
- 59651-408 Memantine HydrochlorideMemantine Hydrochloride Kit by Aurobindo Pharma Limited
- 0121-0850 Memantine Hydrochloride 10 mg/5ml Oral Solution by Pharmaceutical Associates, Inc.
- 0378-1103 Memantine Hydrochloride 5 mg Oral Tablet by Mylan Pharmaceuticals Inc.
- 0378-1104 Memantine Hydrochloride 10 mg Oral Tablet by Mylan Pharmaceuticals Inc.
- 0378-5435 Memantine Hydrochloride 7 mg Oral Capsule, Extended Release by Mylan Pharmaceuticals Inc.
- 0378-5436 Memantine Hydrochloride 14 mg Oral Capsule, Extended Release by Mylan Pharmaceuticals Inc.
- 0378-5437 Memantine Hydrochloride 21 mg Oral Capsule, Extended Release by Mylan Pharmaceuticals Inc.
- 0378-5438 Memantine Hydrochloride 28 mg Oral Capsule, Extended Release by Mylan Pharmaceuticals Inc.
- 0527-1221 Memantine Hydrochloride 5 mg Oral Tablet by Lannett Company, Inc.
- 0527-1222 Memantine Hydrochloride 10 mg Oral Tablet by Lannett Company, Inc.
- 0527-1943 Memantine Hydrochloride 2 mg/ml Oral Solution by Lannett Company, Inc.
- 0591-3011 Memantine Hydrochloride 2 mg/ml Oral Solution by Actavis Pharma, Inc
- 0591-3870 Memantine Hydrochloride 5 mg Oral Tablet by Actavis Pharma, Inc
- 0591-3875 Memantine Hydrochloride 10 mg Oral Tablet by Actavis Pharma, Inc
- 0591-3900 Memantine Hydrochloride Oral Kit by Actavis Pharma, Inc
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.