rexall bismuth
- Product NDC
- 55910-469
- 11-digit product format
- 559100469
- Labeler code
- 55910
- Product ID
- 55910-469_aa37400b-1537-4d3b-9264-1ee62815aafe
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth subsalicylate
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Dolgencorp Inc
- Application
- part335
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-09-28
- Marketing end
- 0000-00-00
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 262 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55910-469 | REXALL BISMUTH (BISMUTH SUBSALICYLATE) TABLET, CHEWABLE [DOLGENCORP INC] | 3 | Legacy NDC | 20160625_cf38b140-a2d0-4970-8cb8-983b96559f69.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55910-469-65 | 55910046965 | 15 BLISTER PACK in 1 CARTON (55910-469-65) > 2 TABLET, CHEWABLE in 1 BLISTER PACK | 15 blister pack | 2012-09-28 | 0000-00-00 | No | No | Current |