72189-221 : Metformin Hydrochloride 850 mg Oral Tablet


NDC72189-221
Labeler: Direct Rx
Product Type: Human Prescription Drug
Drug Name:  Metformin Hydrochloride
Dosage Form: Oral Tablet
Application #: ANDA203769
Rev. Date: 


NDC Package Codes:

  • 72189-221-90: 90 TABLET IN 1 BOTTLE (72189‑221‑90)

Active Ingredients:

  • Metformin Hydrochloride

Dosage Strength:

  • 850 mg

Pharmaceutical Classes:

  • Biguanide [EPC]
  • Biguanides [CS]

Related Products:

Based on records with the same trade name.
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  • 61919-397 Metformin Hydrochloride 1000 mg Oral Tablet by Direct Rx
  • 61919-922 Metformin Hydrochloride 500 mg Oral Tablet, Extended Release by Direct Rx
  • 61919-990 Metformin Hydrochloride 850 mg Oral Tablet by Direct Rx
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  • 0093-1049 Metformin Hydrochloride 850 mg Oral Tablet by Teva Pharmaceuticals USA Inc
  • 0093-7212 Metformin Hydrochloride 750 mg 24 Hr Extended Release Tablet by Teva Pharmaceuticals USA Inc
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  • 0093-7267 Metformin Hydrochloride 500 mg 24 Hr Extended Release Tablet by Teva Pharmaceuticals USA Inc
  • 0179-0178 Metformin Hydrochloride 1000 mg Oral Tablet, Film Coated by Kaiser Foundation Hospitals
  • 0179-0183 Metformin Hydrochloride 850 mg Oral Tablet, Film Coated by Kaiser Foundation Hospitals
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  • 0185-0213 Metformin Hydrochloride 500 mg Oral Tablet by Eon Labs, Inc.
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  • 0185-0221 Metformin Hydrochloride 1 Gm Oral Tablet by Eon Labs, Inc.
  • 0185-4416 Metformin Hydrochloride 500 mg 24 Hr Extended Release Tablet by Eon Labs, Inc.
  • 0228-2657 Metformin Hydrochloride 500 mg Oral Tablet by Actavis Elizabeth LLC
  • More related products ...

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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.