Mefloquine Hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by West-ward Pharmaceuticals Corp. The primary component is Mefloquine Hydrochloride.
| Product ID | 0143-1282_9aaaf269-6535-48d6-be86-eb30c2732a86 |
| NDC | 0143-1282 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Mefloquine Hydrochloride |
| Generic Name | Mefloquine Hydrochloride |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2010-04-21 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA077699 |
| Labeler Name | West-Ward Pharmaceuticals Corp |
| Substance Name | MEFLOQUINE HYDROCHLORIDE |
| Active Ingredient Strength | 250 mg/1 |
| Pharm Classes | Antimalarial [EPC] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| Marketing Start Date | 2010-04-21 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA077699 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-04-21 |
| Marketing End Date | 2014-06-30 |
| Ingredient | Strength |
|---|---|
| MEFLOQUINE HYDROCHLORIDE | 250 mg/1 |
| SPL SET ID: | e513d4f7-2eb3-4eaf-ab5b-a835252b0ae6 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0054-0025 | Mefloquine Hydrochloride | mefloquine hydrochloride |
| 0143-1282 | Mefloquine Hydrochloride | Mefloquine Hydrochloride |
| 0555-0171 | Mefloquine Hydrochloride | Mefloquine Hydrochloride |
| 21695-449 | Mefloquine Hydrochloride | Mefloquine Hydrochloride |
| 21695-561 | Mefloquine Hydrochloride | Mefloquine Hydrochloride |
| 50090-2396 | Mefloquine Hydrochloride | Mefloquine Hydrochloride |
| 52959-803 | Mefloquine Hydrochloride | Mefloquine Hydrochloride |
| 68071-4702 | Mefloquine Hydrochloride | Mefloquine Hydrochloride |
| 68788-6833 | Mefloquine Hydrochloride | Mefloquine Hydrochloride |