Bismuth Subsalicylate

Product NDC
36800-710
11-digit product format
368000710
Labeler code
36800
Product ID
36800-710_ee28191f-5667-4616-e053-2a95a90a62b7
Type
HUMAN OTC DRUG
Nonproprietary name
Bismuth Subsalicylate
Dosage form
CAPSULE, GELATIN COATED
Route
ORAL
Labeler
TOPCO ASSOCIATES LLC
Application
part335
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2021-02-19
Marketing end
0000-00-00
Substance
BISMUTH SUBSALICYLATE
Active strength
262 mg/1
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
36800-710-24Bismuth Subsalicylate12 in 1 BLISTER PACKCAPSULE, GELATIN COATED126
36800-710-24Bismuth Subsalicylate2 in 1 CARTONCAPSULE, GELATIN COATED26

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
36800-710BISMUTH SUBSALICYLATE CAPSULE, GELATIN COATED [TOPCO ASSOCIATES LLC]6Legacy NDC, 2 package rows20250101_629c1b69-9554-415d-9e48-3651838ab78c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2121072bismuth subsalicylate 262 MG Oral CapsulePSN629c1b69-9554-415d-9e48-3651838ab78c6
2121072bismuth subsalicylate 262 MG Oral CapsuleSCD629c1b69-9554-415d-9e48-3651838ab78c6

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
36800-710-24368000710242 BLISTER PACK in 1 CARTON (36800-710-24) > 12 CAPSULE, GELATIN COATED in 1 BLISTER PACK2 blister pack2021-02-190000-00-00NoNoCurrent