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POTASSIUM CHLORIDE
POTASSIUM CHLORIDE - 0121-1465-30 - (POTASSIUM CHLORIDE)
Drug Information of POTASSIUM CHLORIDE
| Product NDC: | 0121-1465 |
| Proprietary Name: | POTASSIUM CHLORIDE |
| Non Proprietary Name: | POTASSIUM CHLORIDE |
| Active Ingredient(s): | 1.5 g/15mL & nbsp; POTASSIUM CHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of POTASSIUM CHLORIDE
| Product NDC: | 0121-1465 |
| Labeler Name: | Pharmaceutical Associates, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19690101 |
Package Information of POTASSIUM CHLORIDE
| Package NDC: | 0121-1465-30 |
| Package Description: | 10 TRAY in 1 CASE (0121-1465-30) > 10 CUP, UNIT-DOSE in 1 TRAY > 30 mL in 1 CUP, UNIT-DOSE |
NDC Information of POTASSIUM CHLORIDE
| NDC Code | 0121-1465-30 |
| Proprietary Name | POTASSIUM CHLORIDE |
| Package Description | 10 TRAY in 1 CASE (0121-1465-30) > 10 CUP, UNIT-DOSE in 1 TRAY > 30 mL in 1 CUP, UNIT-DOSE |
| Product NDC | 0121-1465 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | POTASSIUM CHLORIDE |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19690101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Pharmaceutical Associates, Inc. |
| Substance Name | POTASSIUM CHLORIDE |
| Strength Number | 1.5 |
| Strength Unit | g/15mL |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
