TRIPROLIDINE HYDROCHLORIDE
- Product NDC
- 0536-1258
- 11-digit product format
- 005361258
- Labeler code
- 0536
- Product ID
- 0536-1258_d5f4232f-0e78-f299-e053-2a95a90a0d3f
- 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
- 2019-11-11
- Marketing end
- 2022-04-30
- Substance
- TRIPROLIDINE HYDROCHLORIDE
- Active strength
- 3 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0536-1258-59 | 00536125859 | 237 mL in 1 BOTTLE (0536-1258-59) | 237 ml | 2019-11-11 | 0000-00-00 | No | No | Current |