Meclizine HCl
- Product NDC
- 16571-752
- 11-digit product format
- 165710752
- Labeler code
- 16571
- Product ID
- 16571-752_07ba5b50-4b9f-4ddb-90de-f84bec613344
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MECLIZINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rising Pharma Holdings, Inc.
- Application
- part336
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-08-17
- Marketing end
- 0000-00-00
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Antiemetic [EPC], Emesis Suppression [PE]
- 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 |
|---|
| 16571-752-01 | 16571075201 | 100 TABLET in 1 BOTTLE (16571-752-01) | 100 tablet | 2021-08-17 | 0000-00-00 | No | No | Current |