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Arnica Montana
Arnica Montana - 65111-002-01 - (Arnica Montana)
Drug Information of Arnica Montana
| Product NDC: | 65111-002 |
| Proprietary Name: | Arnica Montana |
| Non Proprietary Name: | Arnica Montana |
| Active Ingredient(s): | 30 [hp_X]/1 & nbsp; Arnica Montana |
| Administration Route(s): | SUBLINGUAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Arnica Montana
| Product NDC: | 65111-002 |
| Labeler Name: | VITAMEDICA INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 19991201 |
Package Information of Arnica Montana
| Package NDC: | 65111-002-01 |
| Package Description: | 1 BLISTER PACK in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK (65111-002-01) > 40 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
NDC Information of Arnica Montana
| NDC Code | 65111-002-01 |
| Proprietary Name | Arnica Montana |
| Package Description | 1 BLISTER PACK in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK (65111-002-01) > 40 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
| Product NDC | 65111-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Arnica Montana |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | SUBLINGUAL |
| Start Marketing Date | 19991201 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | VITAMEDICA INC |
| Substance Name | ARNICA MONTANA |
| Strength Number | 30 |
| Strength Unit | [hp_X]/1 |
| Pharmaceutical Classes |
