Meclizine Hydrochloride
- Product NDC
- 0615-8224
- 11-digit product format
- 006158224
- Labeler code
- 0615
- Product ID
- 0615-8224_d77ce140-ece4-4082-bebe-f4046d24a185
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA201451
- Marketing category
- ANDA
- Marketing start
- 2010-02-12
- 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
- 2020-12-31
- 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 |
|---|
| 0615-8224-39 | 00615822439 | 30 TABLET in 1 BLISTER PACK (0615-8224-39) | 30 tablet | 2018-07-05 | 0000-00-00 | No | No | Current |