Meclizine Hydrochloride
- Product NDC
- 68084-491
- 11-digit product format
- 680840491
- Labeler code
- 68084
- Product ID
- 68084-491_ea3fb07f-0003-8a55-e053-2a95a90a8243
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA201451
- Marketing category
- ANDA
- Marketing start
- 2011-07-14
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68084-491-01 | 68084049101 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-491-01) > 1 TABLET in 1 BLISTER PACK (68084-491-11) | 100 blister pack | 2011-07-14 | 0000-00-00 | No | No | Current |