Mefloquine Hydrochloride
- Product NDC
- 68071-4702
- 11-digit product format
- 680714702
- Labeler code
- 68071
- Product ID
- 68071-4702_bb8bf603-5b01-a093-e053-2a95a90afc12
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mefloquine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA076392
- Marketing category
- ANDA
- Marketing start
- 2004-01-06
- Marketing end
- 0000-00-00
- Substance
- MEFLOQUINE HYDROCHLORIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Antimalarial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68071-4702-8 | 68071470208 | 1 TABLET in 1 BOTTLE (68071-4702-8) | 1 tablet | 2019-01-09 | 0000-00-00 | No | No | Current |