TRIPROLIDINE HYDROCHLORIDE
- Product NDC
- 59556-896
- 11-digit product format
- 595560896
- Labeler code
- 59556
- Product ID
- 59556-896_f431abbd-07cd-4eb3-ba28-3f4ffe906bac
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- triprolidine hydrochloride
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Strides Pharma Inc
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-05-21
- Marketing end
- 0000-00-00
- Substance
- TRIPROLIDINE HYDROCHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record