Meclizine hydrochloride
- Product NDC
- 71205-374
- 11-digit product format
- 712050374
- Labeler code
- 71205
- Product ID
- 71205-374_172c7feb-7576-4840-b2d4-98628075715f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA205136
- Marketing category
- ANDA
- Marketing start
- 2019-04-15
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-374 | MECLIZINE HYDROCHLORIDE TABLET [PROFICIENT RX LP] | 2 | Legacy NDC | 20220722_27e3194c-4ac8-4513-96a2-13972aa815e3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-374-30 | 71205037430 | 30 TABLET in 1 BOTTLE (71205-374-30) | 30 tablet | 2019-12-17 | 0000-00-00 | No | No | Current |
| 71205-374-60 | 71205037460 | 60 TABLET in 1 BOTTLE (71205-374-60) | 60 tablet | 2019-12-17 | 0000-00-00 | No | No | Current |
| 71205-374-90 | 71205037490 | 90 TABLET in 1 BOTTLE (71205-374-90) | 90 tablet | 2019-12-17 | 0000-00-00 | No | No | Current |