TRIPROLIDINE HYDROCHLORIDE
- Product NDC
- 69367-253
- 11-digit product format
- 693670253
- Labeler code
- 69367
- Product ID
- 69367-253_63d97fa4-9b2d-4eef-8865-0cc4af5bc9e8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TRIPROLIDINE HYDROCHLORIDE
- Dosage form
- SYRUP
- Route
- ORAL
- Labeler
- Westminster Pharmaceuticals, LLC
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-03-09
- Substance
- TRIPROLIDINE HYDROCHLORIDE
- Active strength
- .938 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- TRIPROLIDINE HYDROCHLORIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TRIPROLIDINE HYDROCHLORIDE | .938 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | YAN7R5L890 |
| Rxcui | 1491649 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69367-253-30 | TRIPROLIDINE HYDROCHLORIDE | 30 mL in 1 BOTTLE, DROPPER | SYRUP | 30 | | 6 |
| 69367-253-30 | TRIPROLIDINE HYDROCHLORIDE | 1 in 1 CARTON | SYRUP | 1 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69367-253 | TRIPROLIDINE HYDROCHLORIDE SYRUP [WESTMINSTER PHARMACEUTICALS, LLC] | 6 | Current NDC, Legacy NDC, 2 package rows | 20231230_a9f01760-e335-4410-a9b8-8edce2841270.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69367-253-30 | 69367025330 | 1 BOTTLE, DROPPER in 1 CARTON (69367-253-30) / 30 mL in 1 BOTTLE, DROPPER | 2020-03-09 | 0000-00-00 | No | No | Current |