Meclizine Hydrochloride
- Product NDC
- 71335-0732
- 11-digit product format
- 713350732
- Labeler code
- 71335
- Product ID
- 71335-0732_fb50e51f-0e21-497e-864a-0a6b2e9153a6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA201451
- Marketing category
- ANDA
- Marketing start
- 2010-02-12
- Marketing end
- 0000-00-00
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 13 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0732-1 | 71335073201 | 30 TABLET in 1 BOTTLE (71335-0732-1) | 30 tablet | 2015-08-10 | 0000-00-00 | No | No | Current |
| 71335-0732-2 | 71335073202 | 60 TABLET in 1 BOTTLE (71335-0732-2) | 60 tablet | 2015-08-10 | 0000-00-00 | No | No | Current |
| 71335-0732-3 | 71335073203 | 90 TABLET in 1 BOTTLE (71335-0732-3) | 90 tablet | 2015-08-10 | 0000-00-00 | No | No | Current |
| 71335-0732-4 | 71335073204 | 28 TABLET in 1 BOTTLE (71335-0732-4) | 28 tablet | 2015-08-10 | 0000-00-00 | No | No | Current |
| 71335-0732-5 | 71335073205 | 20 TABLET in 1 BOTTLE (71335-0732-5) | 20 tablet | 2015-08-10 | 0000-00-00 | No | No | Current |
| 71335-0732-6 | 71335073206 | 120 TABLET in 1 BOTTLE (71335-0732-6) | 120 tablet | 2015-08-10 | 0000-00-00 | No | No | Current |
| 71335-0732-7 | 71335073207 | 100 TABLET in 1 BOTTLE (71335-0732-7) | 100 tablet | 2018-03-19 | 0000-00-00 | No | No | Current |