Search by Drug Name or NDC
NDC 65219-0008-51 POTASSIUM CHLORIDE 20 meq/50mL Details
POTASSIUM CHLORIDE 20 meq/50mL
POTASSIUM CHLORIDE is a INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Fresenius Kabi USA, LLC. The primary component is POTASSIUM CHLORIDE.
Product Information
| NDC | 65219-0008 |
|---|---|
| Product ID | 65219-008_01f8ade1-6721-4a84-85f6-70da95db049e |
| Associated GPIs | 79700030002070 |
| GCN Sequence Number | 045309 |
| GCN Sequence Number Description | potassium chloride in water PIGGYBACK 20MEQ/50ML INTRAVEN |
| HIC3 | C1D |
| HIC3 Description | POTASSIUM REPLACEMENT |
| GCN | 41331 |
| HICL Sequence Number | 044754 |
| HICL Sequence Number Description | POTASSIUM CHLORIDE IN WATER FOR INJECTION, STERILE |
| Brand/Generic | Generic |
| Proprietary Name | POTASSIUM CHLORIDE |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | POTASSIUM CHLORIDE |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 20 |
| Active Ingredient Units | meq/50mL |
| Substance Name | POTASSIUM CHLORIDE |
| Labeler Name | Fresenius Kabi USA, LLC |
| Pharmaceutical Class | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA211087 |
| Listing Certified Through | 2025-12-31 |
Package
NDC 65219-0008-51 (65219000851)
| NDC Package Code | 65219-008-51 |
|---|---|
| Billing NDC | 65219000851 |
| Package | 60 BAG in 1 CARTON (65219-008-51) / 50 mL in 1 BAG (65219-008-50) |
| Marketing Start Date | 2021-06-25 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |