Bismuth - Subsalicylate 262 mg / 1 Tablet 100 Blister Pack

Reference details for licensed healthcare facility review and verification.

NDC 1148433-0127-10
Product NDC48433-0127
Generic Drug NameBismuth subsalicylate
Brand NameBismuth
ManufacturerSafecor Health, LLC
Strength262 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity100 Blister Pack
Package Description100 BLISTER PACK in 1 BOX, UNIT-DOSE (48433-127-10) / 1 TABLET in 1 BLISTER PACK (48433-127-01)
Active IngredientsBismuth Subsalicylate
Marketing CategoryOTC MONOGRAPH DRUG

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NDC snapshot

Bismuth subsalicylate 262 mg / 1 Tablet is tracked under NDC 48433-0127-10 and rolls up into product family 48433-0127. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 100 Blister Pack.
  • Manufacturer: Safecor Health, LLC.
  • Dosage form: Tablet.
  • Family size: 1 indexed presentation.

Official references

Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.

Bismuth - Subsalicylate 262 mg / 1 Tablet 100 Blister Pack, NDC 48433-0127-10, is a Safecor Health, LLC 262 mg / 1 tablet presentation packaged as 100 Blister Pack.

NDC search formats

  • Canonical NDC 11: 48433-0127-10
  • Digits-only NDC 11: 48433012710
  • Possible 10-digit display format: 48433-127-10 (4843312710)

Helpful product links

  • Search by brand name: Bismuth
  • NDC 11: 48433-0127-10
  • Product family NDC: 48433-0127
  • VA classification code: GA208
  • VA classification code description: ANTIDIARRHEAL AGENTS
  • CMOP ID: B0203
  • VUID: 4009551