47335-322 : Memantine Hydrochloride 10 mg Oral Tablet, Film Coated


NDC: 47335-322
Labeler: Sun Pharma Global Fze
Product Type: Human Prescription Drug
Drug Name:  Memantine Hydrochloride
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA090058
Rev. Date: 


Appearance:


Markings: 322
Shapes:  Capsule
Colors:  Gray
Size (mm): 12
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:

  • 47335-322-08: 100 TABLET, FILM COATED IN 1 BOTTLE (47335‑322‑08)
  • 47335-322-13: 500 TABLET, FILM COATED IN 1 BOTTLE (47335‑322‑13)
  • 47335-322-18: 1000 TABLET, FILM COATED IN 1 BOTTLE (47335‑322‑18)
  • 47335-322-83: 30 TABLET, FILM COATED IN 1 BOTTLE (47335‑322‑83)
  • 47335-322-86: 60 TABLET, FILM COATED IN 1 BOTTLE (47335‑322‑86)
  • 47335-322-88: 100 TABLET, FILM COATED IN 1 BOTTLE (47335‑322‑88)

Active Ingredients:

  • Memantine Hydrochloride

Dosage Strength:

  • 10 mg

Inactive Ingredients:

  • Cellulose, Microcrystalline
  • Anhydrous Lactose
  • Silicon Dioxide
  • Talc
  • Magnesium Stearate
  • Titanium Dioxide
  • Ferrosoferric Oxide
  • Hypromelloses
  • Polyethylene Glycols

Pharmaceutical Classes:

  • NMDA Receptor Antagonists [MoA]
  • N-methyl-D-aspartate Receptor Antagonist [EPC]

Related Products:

Based on records with the same trade name.
  • 47335-321 Memantine Hydrochloride 5 mg Oral Tablet, Film Coated by Sun Pharma Global Fze
  • 47335-031 Memantine Hydrochloride 7 mg Oral Capsule, Extended Release by Sun Pharmaceutical Industries, Inc.
  • 47335-032 Memantine Hydrochloride 14 mg Oral Capsule, Extended Release by Sun Pharmaceutical Industries, Inc.
  • 47335-033 Memantine Hydrochloride 21 mg Oral Capsule, Extended Release by Sun Pharmaceutical Industries, Inc.
  • 47335-034 Memantine Hydrochloride 28 mg Oral Capsule, Extended Release by Sun Pharmaceutical Industries, Inc.
  • 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
  • 0615-8264 Memantine Hydrochloride 28 mg Oral Capsule, Extended Release by Ncs Healthcare of Ky, Inc Dba Vangard Labs
  • More related products ...

NDC QR Code

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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.