Meclizine Hydrochloride
- Product NDC
- 0615-8052
- 11-digit product format
- 006158052
- Labeler code
- 0615
- Product ID
- 0615-8052_07a8baa9-cf70-4008-aef6-ccef0057540c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA200294
- Marketing category
- ANDA
- Marketing start
- 2012-04-30
- Marketing end
- 2020-04-30
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Antiemetic [EPC],Emesis Suppression [PE]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record