0093-7037 : Amlodipine, Valsartan, and Hydrochlorothiazide Oral Tablet, Film Coated


NDC0093-7037
Labeler: Teva Pharmaceuticals USA Inc
Product Type: Human Prescription Drug
Drug Name: Amlodipine, Valsartan, and Hydrochlorothiazide
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA200435
Rev. Date: 


Appearance:


Markings: TV;7037
Shapes:  Round
Colors:  Yellow
Size (mm): 11
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.

TV 7037: (0093-7037) Amlodipine, Valsartan, and Hydrochlorothiazide Oral Tablet, Film Coated by Teva Pharmaceuticals USA Inc
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

  • 0093-7037-56: 30 TABLET, FILM COATED IN 1 BOTTLE (0093‑7037‑56)
  • 0093-7037-98: 90 TABLET, FILM COATED IN 1 BOTTLE (0093‑7037‑98)

Active Ingredients:

  • Amlodipine Besylate
  • Valsartan
  • Hydrochlorothiazide

Dosage Strength:

  • 5 mg
  • 160 mg
  • 25 mg

Inactive Ingredients:

  • Calcium Phosphate, Dibasic, Anhydrous
  • Silicon Dioxide
  • Crospovidone
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Polyethylene Glycol 3350
  • Polyethylene Glycol 4000
  • Polyvinyl Alcohol
  • Sodium Starch Glycolate Type a Potato
  • Starch, Corn
  • Talc
  • Titanium Dioxide
  • Ferric Oxide Yellow

Pharmaceutical Classes:

  • Calcium Channel Antagonists [MoA]
  • Dihydropyridine Calcium Channel Blocker [EPC]
  • Dihydropyridines [CS]
  • Angiotensin 2 Receptor Antagonists [MoA]
  • Angiotensin 2 Receptor Blocker [EPC]
  • Increased Diuresis [PE]
  • Thiazide Diuretic [EPC]
  • Thiazides [CS]

Related Products:

Based on records with the same trade name.
  • 0093-7038 Amlodipine, Valsartan, and Hydrochlorothiazide Oral Tablet, Film Coated by Teva Pharmaceuticals USA Inc
  • 0093-7807 Amlodipine, Valsartan, and Hydrochlorothiazide Oral Tablet, Film Coated by Teva Pharmaceuticals USA Inc
  • 0093-7809 Amlodipine, Valsartan, and Hydrochlorothiazide Oral Tablet, Film Coated by Teva Pharmaceuticals USA Inc
  • 0093-7810 Amlodipine, Valsartan, and Hydrochlorothiazide Oral Tablet, Film Coated by Teva Pharmaceuticals USA Inc
  • 13668-325 Amlodipine, Valsartan and Hydrochlorothiazide Oral Tablet by Torrent Pharmaceuticals Limited
  • 13668-326 Amlodipine, Valsartan and Hydrochlorothiazide Oral Tablet by Torrent Pharmaceuticals Limited
  • 13668-327 Amlodipine, Valsartan and Hydrochlorothiazide Oral Tablet by Torrent Pharmaceuticals Limited
  • 13668-328 Amlodipine, Valsartan and Hydrochlorothiazide Oral Tablet by Torrent Pharmaceuticals Limited
  • 13668-329 Amlodipine, Valsartan and Hydrochlorothiazide Oral Tablet by Torrent Pharmaceuticals Limited
  • 57297-771 Amlodipine, Valsartan and Hydrochlorothiazide Oral Tablet, Film Coated by Lupin Limited
  • 57297-772 Amlodipine, Valsartan and Hydrochlorothiazide Oral Tablet, Film Coated by Lupin Limited
  • 57297-773 Amlodipine, Valsartan and Hydrochlorothiazide Oral Tablet, Film Coated by Lupin Limited
  • 57297-774 Amlodipine, Valsartan and Hydrochlorothiazide Oral Tablet, Film Coated by Lupin Limited
  • 57297-775 Amlodipine, Valsartan and Hydrochlorothiazide Oral Tablet, Film Coated by Lupin Limited
  • 65862-834 Amlodipine, Valsartan and Hydrochlorothiazide Oral Tablet, Film Coated by Aurobindo Pharma Limited
  • 65862-835 Amlodipine, Valsartan and Hydrochlorothiazide Oral Tablet, Film Coated by Aurobindo Pharma Limited
  • 65862-836 Amlodipine, Valsartan and Hydrochlorothiazide Oral Tablet, Film Coated by Aurobindo Pharma Limited
  • 65862-837 Amlodipine, Valsartan and Hydrochlorothiazide Oral Tablet, Film Coated by Aurobindo Pharma Limited
  • 65862-838 Amlodipine, Valsartan and Hydrochlorothiazide Oral Tablet, Film Coated by Aurobindo Pharma Limited
  • 68180-771 Amlodipine, Valsartan and Hydrochlorothiazide Oral Tablet, Film Coated by Lupin Pharmaceuticals, Inc.
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NDC QR Code

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NDC 0093-7037 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.