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CHLORALUM
CHLORALUM - 10191-1177-2 - (CHLORAL HYDRATE)
Drug Information of CHLORALUM
| Product NDC: | 10191-1177 |
| Proprietary Name: | CHLORALUM |
| Non Proprietary Name: | CHLORAL HYDRATE |
| Active Ingredient(s): | 3 [hp_X]/1 & nbsp; CHLORAL HYDRATE |
| Administration Route(s): | SUBLINGUAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CHLORALUM
| Product NDC: | 10191-1177 |
| Labeler Name: | Remedy Makers |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20000204 |
Package Information of CHLORALUM
| Package NDC: | 10191-1177-2 |
| Package Description: | 172 PELLET in 1 VIAL, GLASS (10191-1177-2) |
NDC Information of CHLORALUM
| NDC Code | 10191-1177-2 |
| Proprietary Name | CHLORALUM |
| Package Description | 172 PELLET in 1 VIAL, GLASS (10191-1177-2) |
| Product NDC | 10191-1177 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CHLORAL HYDRATE |
| Dosage Form Name | PELLET |
| Route Name | SUBLINGUAL |
| Start Marketing Date | 20000204 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Remedy Makers |
| Substance Name | CHLORAL HYDRATE |
| Strength Number | 3 |
| Strength Unit | [hp_X]/1 |
| Pharmaceutical Classes |
