Motion sickness
- Product NDC
- 50804-620
- 11-digit product format
- 508040620
- Labeler code
- 50804
- Product ID
- 50804-620_2c0e4942-17ab-47f2-a2d0-d1336b636f8b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Meclizine HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Good Sense (Geiss, Destin & Dunn, Inc.)
- Application
- part336
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-03-19
- Marketing end
- 2023-12-31
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 50804-620-08 | 50804062008 | 1 BLISTER PACK in 1 CARTON (50804-620-08) > 8 TABLET in 1 BLISTER PACK | 1 blister pack | 2012-03-19 | 2023-12-31 | No | No | Current |