72205-087 : Tiagabine Hydrochloride 16 mg Oral Tablet


NDC: 72205-087
Labeler: Novadoz Pharmaceuticals LLC
Product Type: Human Prescription Drug
Drug Name:  Tiagabine Hydrochloride
Dosage Form: Oral Tablet
Application #: ANDA214816
Rev. Date: 


NDC Package Codes:

  • 72205-087-30: 30 TABLET IN 1 BOTTLE (72205‑087‑30)

Active Ingredients:

  • Tiagabine Hydrochloride

Dosage Strength:

  • 16 mg

Pharmaceutical Classes:

  • Anti-epileptic Agent [EPC]
  • Decreased Central Nervous System Disorganized Electrical Activity [PE]

Related Products:

Based on records with the same trade name.
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  • 0093-5030 Tiagabine Hydrochloride 2 mg Oral Tablet, Film Coated by Teva Pharmaceuticals USA, Inc.
  • 0093-5031 Tiagabine Hydrochloride 4 mg Oral Tablet, Film Coated by Teva Pharmaceuticals USA, Inc.
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  • 0093-8076 Tiagabine Hydrochloride 16 mg Oral Tablet, Film Coated by Teva Pharmaceuticals USA, Inc.
  • 16714-151 Tiagabine Hydrochloride 2 mg Oral Tablet by Northstar Rx LLC
  • 16714-152 Tiagabine Hydrochloride 4 mg Oral Tablet by Northstar Rx LLC
  • 16714-153 Tiagabine Hydrochloride 12 mg Oral Tablet by Northstar Rx LLC
  • 16714-154 Tiagabine Hydrochloride 16 mg Oral Tablet by Northstar Rx LLC
  • 52536-350 Tiagabine Hydrochloride 2 mg Oral Tablet by Wilshire Pharmaceuticals, Inc.
  • 52536-355 Tiagabine Hydrochloride 4 mg Oral Tablet by Wilshire Pharmaceuticals, Inc.
  • 52536-360 Tiagabine Hydrochloride 12 mg Oral Tablet by Wilshire Pharmaceuticals, Inc.
  • 52536-365 Tiagabine Hydrochloride 16 mg Oral Tablet by Wilshire Pharmaceuticals, Inc.
  • 55253-600 Tiagabine Hydrochloride 2 mg Oral Tablet by Cima Laboratories, Inc.
  • 55253-601 Tiagabine Hydrochloride 4 mg Oral Tablet by Cima Laboratories, Inc.
  • 62756-200 Tiagabine Hydrochloride 2 mg Oral Tablet by Sun Pharmaceutical Industries Limited
  • 62756-224 Tiagabine Hydrochloride 4 mg Oral Tablet by Sun Pharmaceutical Industries Limited
  • 69189-0602 Tiagabine Hydrochloride 4 mg Oral Tablet, Film Coated by Avera Mckennan Hospital
  • More related products ...

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