Meclizine Hydrochloride
- Product NDC
- 68788-7873
- 11-digit product format
- 687887873
- Labeler code
- 68788
- Product ID
- 68788-7873_cd73003a-7807-4fe4-9a7c-96534c29ac27
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- M009
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-02-19
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Meclizine Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MECLIZINE HYDROCHLORIDE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | HDP7W44CIO |
| Rxcui | 995632 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7873-1 | 68788787301 | 100 TABLET, CHEWABLE in 1 BOTTLE (68788-7873-1) | 2021-02-19 | 0000-00-00 | No | No | Current |
| 68788-7873-2 | 68788787302 | 30 TABLET, CHEWABLE in 1 BOTTLE (68788-7873-2) | 2022-08-26 | 0000-00-00 | No | No | Current |
| 68788-7873-3 | 68788787303 | 1000 TABLET, CHEWABLE in 1 BOTTLE (68788-7873-3) | 2021-02-19 | 0000-00-00 | No | No | Current |