Bismuth Subsalicylate
- Product NDC
- 68210-4152
- 11-digit product format
- 682104152
- Labeler code
- 68210
- Product ID
- 68210-4152_ee8f10a2-cd95-b261-e053-2995a90a30bf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth Subsalicylate
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- Spirit Pharmaceuticals LLC
- Application
- part335
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-04-29
- 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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68210-4152-1 | Bismuth Subsalicylate | 1 in 1 CARTON | CAPSULE, GELATIN COATED | 1 | | 5 |
| 68210-4152-1 | Bismuth Subsalicylate | 12 in 1 BLISTER PACK | CAPSULE, GELATIN COATED | 12 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68210-4152 | BISMUTH SUBSALICYLATE CAPSULE, GELATIN COATED [SPIRIT PHARMACEUTICALS LLC] | 5 | Legacy NDC, 2 package rows | 20241213_86e7d60c-6900-46b4-9c70-c0d8fb6bd420.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68210-4152-1 | 68210415201 | 1 BLISTER PACK in 1 CARTON (68210-4152-1) > 12 CAPSULE, GELATIN COATED in 1 BLISTER PACK | 1 blister pack | 2021-04-29 | 0000-00-00 | No | No | Current |