Product NDC: | 60512-1035 |
Proprietary Name: | NUX VOMICA |
Non Proprietary Name: | NUX VOMICA |
Active Ingredient(s): | 3 [hp_X]/1 & nbsp; NUX VOMICA |
Administration Route(s): | ORAL |
Dosage Form(s): | PELLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60512-1035 |
Labeler Name: | HOMEOLAB USA INC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 19951011 |
Package NDC: | 60512-1035-1 |
Package Description: | 80 PELLET in 1 TUBE (60512-1035-1) |
NDC Code | 60512-1035-1 |
Proprietary Name | NUX VOMICA |
Package Description | 80 PELLET in 1 TUBE (60512-1035-1) |
Product NDC | 60512-1035 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | NUX VOMICA |
Dosage Form Name | PELLET |
Route Name | ORAL |
Start Marketing Date | 19951011 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | HOMEOLAB USA INC |
Substance Name | STRYCHNOS NUX-VOMICA SEED |
Strength Number | 3 |
Strength Unit | [hp_X]/1 |
Pharmaceutical Classes |