Triprolidine Hydrochloride
- Product NDC
- 69367-186
- 11-digit product format
- 693670186
- Labeler code
- 69367
- Product ID
- 69367-186_bf5f0dbe-a803-42e4-a343-3d718ac5428f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TRIPROLIDINE HYDROCHLORIDE
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Westminster Pharmaceuticals, LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-03-15
- Marketing end
- 0000-00-00
- Substance
- TRIPROLIDINE HYDROCHLORIDE
- Active strength
- 0 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69367-186-50 | 69367018650 | 1 BOTTLE in 1 CARTON (69367-186-50) > 50 mL in 1 BOTTLE | 1 bottle | 2018-03-15 | 0000-00-00 | No | No | Current |