Allerdine
- Product NDC
- 69784-803
- 11-digit product format
- 697840803
- Labeler code
- 69784
- Product ID
- 69784-803_cc2edd3d-bf9f-40cf-8ad8-0b70d5b77a88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TRIPROLIDINE HYDROCHLORIDE
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Woodward Pharma Services LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-06-09
- Marketing end
- 0000-00-00
- Substance
- TRIPROLIDINE HYDROCHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record