Mefloquine Hydrochloride
- Product NDC
- 68788-6833
- 11-digit product format
- 687886833
- Labeler code
- 68788
- Product ID
- 68788-6833_08f5651a-bffe-4e46-9808-39a4f8101bba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mefloquine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA076392
- Marketing category
- ANDA
- Marketing start
- 2016-11-21
- Marketing end
- 0000-00-00
- Substance
- MEFLOQUINE HYDROCHLORIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Antimalarial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 68788-6833-2 | 68788683302 | 25 BLISTER PACK in 1 CARTON (68788-6833-2) > 1 TABLET in 1 BLISTER PACK | 25 blister pack | 2016-11-21 | 0000-00-00 | No | No | Current |