Home NDC 64950-320 Potassium Chloride
Product NDC 64950-320
11-digit product format 649500320
Labeler code 64950
Product ID 64950-320_2fe5566d-af35-4b1a-8ed6-a7b803dfc896
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Potassium Chloride
Dosage form SOLUTION
Route ORAL
Labeler Genus Lifesciences
Application NDA206814
Marketing category NDA
Marketing start 2015-02-15
Marketing end 2027-09-30
Substance POTASSIUM CHLORIDE
Active strength 20 meq/15mL
Pharmacologic classes Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
NDC exclude flag No
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 7 matching rows.
View current auxiliary records. · View the auxiliary file history.
Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 3 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date N206814-001 POTASSIUM CHLORIDE POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 N206814-002 POTASSIUM CHLORIDE POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 N206814-003 POKONZA POTASSIUM CHLORIDE 10MEQ/15ML SOLUTION / ORAL RLD 2025-11-25
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 2 matching rows.
Orange Book patents# Current patent rows page 1 of 1 · 2 matching rows.
Application-product, Patent, Expiration table Application-product Patent Expiration Use code Coverage / status Submission date N206814-001 12539314 2039-03-07 Drug product 2026-02-04 N206814-002 12539314 2039-03-07 Drug product 2026-02-04
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Product history page 1 of 3 · 85 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-02-19 14:30 UTC 2026-02 N206814-001 POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N206814-002 POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N206814-003 POKONZA 10MEQ/15ML SOLUTION / ORAL RLD 2025-11-25 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N206814-001 POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N206814-002 POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N206814-003 POKONZA 10MEQ/15ML SOLUTION / ORAL RLD 2025-11-25 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 N206814-001 POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N206814-002 POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N206814-001 POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N206814-002 POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N206814-001 POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N206814-002 POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N206814-001 POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N206814-002 POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N206814-001 POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N206814-002 POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N206814-001 POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N206814-002 POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N206814-001 POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N206814-002 POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 N206814-001 POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 d06236e962d9…2024-10-29 15:01 UTC 2024-10 N206814-002 POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N206814-001 POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N206814-002 POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 N206814-001 POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 301d65b070ca…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 N206814-002 POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 N206814-001 POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 1e350fbaab3a…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 N206814-002 POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 1e350fbaab3a…2024-05-31 18:47 UTC 2024-05 N206814-001 POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 8072bd15b7f6…2024-05-31 18:47 UTC 2024-05 N206814-002 POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 8072bd15b7f6…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 N206814-001 POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 5c6f7cd8ea54…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 N206814-002 POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 5c6f7cd8ea54…2022-04-08 23:34 UTC 2022-04 N206814-001 POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 5d02ea3f76ae…2022-04-08 23:34 UTC 2022-04 N206814-002 POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 5d02ea3f76ae…2022-04-04 05:41 UTC 2022-04 N206814-001 POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 4b0b4de00fa7…2022-04-04 05:41 UTC 2022-04 N206814-002 POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 4b0b4de00fa7…2019-12-13 00:20 UTC 2019-12 N206814-001 POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 74a2ff9319b5…2019-12-13 00:20 UTC 2019-12 N206814-002 POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 74a2ff9319b5…2022-03-09 01:35 UTC 2022-03 N206814-001 POTASSIUM CHLORIDE 20MEQ/15ML SOLUTION / ORAL AA RLD 2014-12-22 bb7c543d1eb4…2022-03-09 01:35 UTC 2022-03 N206814-002 POTASSIUM CHLORIDE 40MEQ/15ML SOLUTION / ORAL AA RLD, RS 2014-12-22 bb7c543d1eb4…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 3 · 82 observed states.
Observed Orange Book patent history# Captured, Edition, Application-product table Captured Edition Application-product Patent Expiration Use code Coverage / status Submission date Source SHA-256 2026-02-19 14:30 UTC 2026-02 N206814-001 12539314 2039-03-07 Drug product 2026-02-04 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N206814-002 12539314 2039-03-07 Drug product 2026-02-04 011fe1cb6892…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 N206814-001 12539314 2039-03-07 Drug product 2026-02-04 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 N206814-002 12539314 2039-03-07 Drug product 2026-02-04 a50c72e98297…
Additional Listing Data#
Finished product Yes
Brand name base Potassium Chloride Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM CHLORIDE 20 meq/15mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 660YQ98I10 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 312515 Internal RxNorm lookup 314182 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 64950-320-47 Potassium Chloride 473 mL in 1 BOTTLE, PLASTIC SOLUTION 473 11 64950-320-99 Potassium Chloride 113562 mL in 1 DRUM SOLUTION 113562 11
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Potassium Chloride ACTIVE INGREDIENT 660YQ98I10 POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.] 1 Potassium Chloride ACTIVE INGREDIENT 660YQ98I10 POTASSIUM CHLORIDE SOLUTION [LEHIGH VALLEY TECHNOLOGIES, INC.] 1 Chloride Ion ACTIVE MOIETY Q32ZN48698 POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.] 1 Chloride Ion ACTIVE MOIETY Q32ZN48698 POTASSIUM CHLORIDE SOLUTION [LEHIGH VALLEY TECHNOLOGIES, INC.] 1 Anhydrous Citric Acid INACTIVE INGREDIENT XF417D3PSL POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.] 1 Anhydrous Citric Acid INACTIVE INGREDIENT XF417D3PSL POTASSIUM CHLORIDE SOLUTION [LEHIGH VALLEY TECHNOLOGIES, INC.] 1 FD&C Yellow NO. 6 INACTIVE INGREDIENT H77VEI93A8 POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.] 1 FD&C Yellow NO. 6 INACTIVE INGREDIENT H77VEI93A8 POTASSIUM CHLORIDE SOLUTION [LEHIGH VALLEY TECHNOLOGIES, INC.] 1 Glycerin INACTIVE INGREDIENT PDC6A3C0OX POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.] 1 Glycerin INACTIVE INGREDIENT PDC6A3C0OX POTASSIUM CHLORIDE SOLUTION [LEHIGH VALLEY TECHNOLOGIES, INC.] 1 Methylparaben INACTIVE INGREDIENT A2I8C7HI9T POTASSIUM CHLORIDE SOLUTION [LEHIGH VALLEY TECHNOLOGIES, INC.] 1 Methylparaben INACTIVE INGREDIENT A2I8C7HI9T POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.] 1 Propylene Glycol INACTIVE INGREDIENT 6DC9Q167V3 POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.] 1 Propylene Glycol INACTIVE INGREDIENT 6DC9Q167V3 POTASSIUM CHLORIDE SOLUTION [LEHIGH VALLEY TECHNOLOGIES, INC.] 1 Propylparaben INACTIVE INGREDIENT Z8IX2SC1OH POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.] 1 Propylparaben INACTIVE INGREDIENT Z8IX2SC1OH POTASSIUM CHLORIDE SOLUTION [LEHIGH VALLEY TECHNOLOGIES, INC.] 1 Sodium Citrate INACTIVE INGREDIENT 1Q73Q2JULR POTASSIUM CHLORIDE SOLUTION [LEHIGH VALLEY TECHNOLOGIES, INC.] 1 Sucralose INACTIVE INGREDIENT 96K6UQ3ZD4 POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.] 1 Sucralose INACTIVE INGREDIENT 96K6UQ3ZD4 POTASSIUM CHLORIDE SOLUTION [LEHIGH VALLEY TECHNOLOGIES, INC.] 1 Trisodium Citrate Dihydrate INACTIVE INGREDIENT B22547B95K POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.] 1 Water INACTIVE INGREDIENT 059QF0KO0R POTASSIUM CHLORIDE SOLUTION [LEHIGH VALLEY TECHNOLOGIES, INC.] 1 Water INACTIVE INGREDIENT 059QF0KO0R POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 64950-320 POTASSIUM CHLORIDE SOLUTION [GENUS LIFESCIENCES] 8 Current NDC, Legacy NDC, 2 package rows 20250124_14cd12ee-a4a3-465a-9550-58c9ef0e4f21.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 3 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 64950-320-47 64950032047 473 mL in 1 BOTTLE, PLASTIC (64950-320-47) 473 ml 2015-02-15 2027-09-30 No No Historical 64950-320-99 64950032099 113562 mL in 1 DRUM (64950-320-99) 113562 ml 2016-01-21 0000-00-00 No No Current