62211-046 : Bismuth Subsalicylate 262 mg Chewable Tablet


NDC: 62211-046
Labeler: A&z Pharmaceutical, Inc.
Product Type: Human OTC Drug
Drug Name:  Bismuth Subsalicylate
Dosage Form: Oral Tablet, Chewable
Application #: part335
Rev. Date: 


Appearance:


Markings: AZ046
Shapes:  Round
Colors:  Pink
Size (mm): 16
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:

  • 62211-046-18: 18 TABLET, CHEWABLE IN 1 CELLO PACK (62211‑046‑18)
  • 62211-046-69: 12 TABLET, CHEWABLE IN 1 CELLO PACK (62211‑046‑69)
  • 62211-046-88: 30 TABLET, CHEWABLE IN 1 CELLO PACK (62211‑046‑88)
  • 62211-046-99: 15000 TABLET, CHEWABLE IN 1 CARTON (62211‑046‑99)

Active Ingredients:

  • Bismuth Subsalicylate

Dosage Strength:

  • 262 mg

Inactive Ingredients:

  • Aspartame
  • Calcium Carbonate
  • D&c Red No. 27
  • Magnesium Stearate

Related Products:

Based on records with the same trade name.
  • 0536-4301 Bismuth Subsalicylate 262 mg Oral Tablet by Rugby Laboratories Inc.
  • 36800-710 Bismuth Subsalicylate 262 mg Oral Capsule, Gelatin Coated by Topco Associates LLC
  • 68071-4523 Bismuth Subsalicylate 262 mg Oral Tablet, Chewable by Nucare Pharmaceuticals, Inc.
  • 68210-4152 Bismuth Subsalicylate 262 mg Oral Capsule, Gelatin Coated by Spirit Pharmaceuticals LLC
  • 68210-5018 Bismuth Subsalicylate 262 mg Oral Capsule, Gelatin Coated by Spirit Pharmaceuticals LLC
  • 69168-999 Bismuth Subsalicylate 262 mg Oral Tablet, Chewable by Allegiant Health
  • 69842-346 Bismuth Subsalicylate 262 mg Oral Tablet, Film Coated by Cvs Pharmacy, Inc.
  • 69842-799 Bismuth Subsalicylate 262 mg Oral Capsule, Gelatin Coated by Cvs Pharmacy, Inc.
  • 70000-0594 Bismuth Subsalicylate 262 mg Oral Tablet, Film Coated by Cardinal Health
  • 70166-059 Bismuth Subsalicylate 262 mg/15ml Oral Liquid by Lohxa

NDC QR Code

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NDC 62211-046 QR Code

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Related Discussions:

composition of bismuth subsalicylate drug
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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.