Bismuth Subsalicylate 262 mg
- Product NDC
- 68788-8128
- 11-digit product format
- 687888128
- Labeler code
- 68788
- Product ID
- 68788-8128_a8f6bd6f-e972-434e-b0de-ab65b67a1ce4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth Subsalicylate
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- part335
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2022-02-03
- Marketing end
- 0000-00-00
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 262 mg/1
- Pharmacologic classes
- Bismuth [CS], Bismuth [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8128-3 | 68788812803 | 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (68788-8128-3) | 2022-02-03 | 0000-00-00 | No | No | Current |