71993-309 : Tolmetin Sodium 400 mg Oral Capsule


NDC: 71993-309
Labeler: Atland Pharmaceuticals, LLC
Product Type: Human Prescription Drug
Drug Name:  Tolmetin Sodium
Dosage Form: Oral Capsule
Application #: ANDA073393
Rev. Date: 


NDC Package Codes:

  • 71993-309-30: 30 CAPSULE IN 1 BOTTLE (71993‑309‑30)

Active Ingredients:

  • Tolmetin Sodium

Dosage Strength:

  • 400 mg

Pharmaceutical Classes:

  • Anti-Inflammatory Agents
  • Non-Steroidal [CS]
  • Cyclooxygenase Inhibitors [MoA]
  • Nonsteroidal Anti-inflammatory Drug [EPC]

Related Products:

Based on records with the same trade name.
  • 0093-2075 Tolmetin 400 mg (As Tolmetin Sodium Dihydrate 492 mg) Oral Capsule by Teva Pharmaceuticals USA Inc
  • 0093-8815 Tolmetin 400 mg (As Tolmetin Sodium Dihydrate 492 mg) Oral Capsule by Teva Pharmaceuticals USA Inc
  • 0378-0313 Tolmetin 600 mg Oral Tablet by Mylan Pharmaceuticals Inc.
  • 0378-5200 Tolmetin 400 mg (As Tolmetin Sodium Dihydrate 492 mg) Oral Capsule by Mylan Pharmaceuticals Inc.
  • 16571-825 Tolmetin Sodium 600 mg Oral Tablet, Film Coated by Rising Pharma Holdings, Inc.
  • 16571-826 Tolmetin Sodium 400 mg Oral Capsule by Rising Pharma Holdings, Inc.
  • 16590-987 Tolmetin 600 mg Oral Tablet by Stat Rx USA LLC
  • 53489-506 Tolmetin 200 mg Oral Tablet by Mutual Pharmaceutical Company, Inc.
  • 53489-507 Tolmetin 400 mg (As Tolmetin Sodium Dihydrate 492 mg) Oral Capsule by Mutual Pharmaceutical Company, 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.