Motion Sickness
- Product NDC
- 50804-630
- 11-digit product format
- 508040630
- Labeler code
- 50804
- Product ID
- 50804-630_42512fa9-7764-4275-808a-e2cd26d653a0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dimenhydrinate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Good Sense (Geiss, Destin & Dunn, Inc.)
- Application
- part336
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2010-08-10
- Marketing end
- 2021-12-30
- Substance
- DIMENHYDRINATE
- Active strength
- 50 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 |
|---|
| 50804-630-12 | 50804063012 | 1 BLISTER PACK in 1 CARTON (50804-630-12) > 12 TABLET in 1 BLISTER PACK | 1 blister pack | 2010-08-10 | 2021-12-30 | No | No | Current |