Home
>
National Drug Code (NDC)
>
Sulphur
Sulphur - 53499-7172-2 - (SULFUR)
Drug Information of Sulphur
| Product NDC: | 53499-7172 |
| Proprietary Name: | Sulphur |
| Non Proprietary Name: | SULFUR |
| Active Ingredient(s): | 30 [hp_X]/1 & nbsp; SULFUR |
| Administration Route(s): | SUBLINGUAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sulphur
| Product NDC: | 53499-7172 |
| Labeler Name: | Nature's Way Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20040701 |
Package Information of Sulphur
| Package NDC: | 53499-7172-2 |
| Package Description: | 100 TABLET in 1 BOTTLE, GLASS (53499-7172-2) |
NDC Information of Sulphur
| NDC Code | 53499-7172-2 |
| Proprietary Name | Sulphur |
| Package Description | 100 TABLET in 1 BOTTLE, GLASS (53499-7172-2) |
| Product NDC | 53499-7172 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SULFUR |
| Dosage Form Name | TABLET |
| Route Name | SUBLINGUAL |
| Start Marketing Date | 20040701 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Nature's Way Products, Inc. |
| Substance Name | SULFUR |
| Strength Number | 30 |
| Strength Unit | [hp_X]/1 |
| Pharmaceutical Classes |
