TRIPROLIDINE HYDROCHLORIDE
- Product NDC
- 0536-1257
- 11-digit product format
- 005361257
- Labeler code
- 0536
- Product ID
- 0536-1257_d5f3e7c2-4d87-f400-e053-2995a90ad67d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TRIPROLIDINE HYDROCHLORIDE
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Rugby Laboratories
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-11-09
- Marketing end
- 0000-00-00
- Substance
- TRIPROLIDINE HYDROCHLORIDE
- Active strength
- 1 mg/mL
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0536-1257-75 | 00536125775 | 30 mL in 1 BOTTLE, DROPPER (0536-1257-75) | 30 ml | 2019-11-09 | 0000-00-00 | No | No | Current |