Meclizine Hydrochloride
- Product NDC
- 70518-2074
- 11-digit product format
- 705182074
- Labeler code
- 70518
- Product ID
- 70518-2074_97204948-ee04-95ec-e053-2a95a90a8df8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA201451
- Marketing category
- ANDA
- Marketing start
- 2019-05-13
- 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