Treda Ultra
- Product NDC
- 83393-749
- 11-digit product format
- 833930749
- Labeler code
- 83393
- Product ID
- 83393-749_bf8d9411-58f5-4b37-8af1-6b7142172ef2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth subsalicylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Laboratorios Sanfer, S.A. de C.V.
- Application
- M008
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-02-06
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 525 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Treda Ultra
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BISMUTH SUBSALICYLATE | 525 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 62TEY51RR1 |
| Rxcui | 1998447 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 83393-749-08 | Treda Ultra | 1 in 1 CARTON | TABLET | 1 | | 3 |
| 83393-749-08 | Treda Ultra | 24 in 1 BOTTLE, PLASTIC | TABLET | 24 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 83393-749 | TREDA ULTRA (BISMUTH SUBSALICYLATE) TABLET [LABORATORIOS SANFER, S.A. DE C.V.] | 2 | Current NDC, 2 package rows | 20250217_cfa7f37a-e18b-4929-b3a4-4126b0aa679a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 83393-749-08 | 83393074908 | 1 BOTTLE, PLASTIC in 1 CARTON (83393-749-08) / 24 TABLET in 1 BOTTLE, PLASTIC | 2024-02-06 | No | No | Historical |