Product NDC: | 54973-3106 |
Proprietary Name: | KALI PHOS |
Non Proprietary Name: | POTASSIUM PHOSPHATE, UNSPECIFIED FORM |
Active Ingredient(s): | 30 [hp_X]/1 & nbsp; POTASSIUM PHOSPHATE, UNSPECIFIED FORM |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54973-3106 |
Labeler Name: | Hyland's |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 19400101 |
Package NDC: | 54973-3106-2 |
Package Description: | 1000 TABLET in 1 BOTTLE, PLASTIC (54973-3106-2) |
NDC Code | 54973-3106-2 |
Proprietary Name | KALI PHOS |
Package Description | 1000 TABLET in 1 BOTTLE, PLASTIC (54973-3106-2) |
Product NDC | 54973-3106 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | POTASSIUM PHOSPHATE, UNSPECIFIED FORM |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19400101 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Hyland's |
Substance Name | POTASSIUM PHOSPHATE, UNSPECIFIED FORM |
Strength Number | 30 |
Strength Unit | [hp_X]/1 |
Pharmaceutical Classes |