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Mefloquine Hydrochloride
Mefloquine Hydrochloride - 0781-5076-86 - (Mefloquine Hydrochloride)
Drug Information of Mefloquine Hydrochloride
| Product NDC: | 0781-5076 |
| Proprietary Name: | Mefloquine Hydrochloride |
| Non Proprietary Name: | Mefloquine Hydrochloride |
| Active Ingredient(s): | 250 mg/1 & nbsp; Mefloquine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mefloquine Hydrochloride
| Product NDC: | 0781-5076 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076175 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020220 |
Package Information of Mefloquine Hydrochloride
| Package NDC: | 0781-5076-86 |
| Package Description: | 5 BLISTER PACK in 1 DOSE PACK (0781-5076-86) > 5 TABLET in 1 BLISTER PACK |
NDC Information of Mefloquine Hydrochloride
| NDC Code | 0781-5076-86 |
| Proprietary Name | Mefloquine Hydrochloride |
| Package Description | 5 BLISTER PACK in 1 DOSE PACK (0781-5076-86) > 5 TABLET in 1 BLISTER PACK |
| Product NDC | 0781-5076 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Mefloquine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20020220 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | MEFLOQUINE HYDROCHLORIDE |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antimalarial [EPC] |
