Meclizine Hydrochloride
- Product NDC
- 71610-836
- 11-digit product format
- 716100836
- Labeler code
- 71610
- Product ID
- 71610-836_1a8bdae4-1b42-0a1c-e063-6294a90a49aa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- M009
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-10-30
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Antiemetic [EPC], Emesis Suppression [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| HDP7W44CIO | MECLIZINE HYDROCHLORIDE | 31884-77-2 | MECLIZINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71610-836-30 | 71610083630 | 30 TABLET, CHEWABLE in 1 BOTTLE (71610-836-30) | 2024-05-24 | No | No | Historical |
| 71610-836-53 | 71610083653 | 60 TABLET, CHEWABLE in 1 BOTTLE (71610-836-53) | 2024-05-24 | No | No | Historical |
| 71610-836-60 | 71610083660 | 90 TABLET, CHEWABLE in 1 BOTTLE (71610-836-60) | 2024-05-24 | No | No | Historical |
| 71610-836-80 | 71610083680 | 180 TABLET, CHEWABLE in 1 BOTTLE (71610-836-80) | 2024-05-24 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| 5172C- Rubgy | Aphena Pharma Solutions - Tennessee, LLC | 2024-06-10 | HUMAN OTC DRUG LABEL | 2 |