Home NDC 66758-140-81 KLOR-CON/EF
Product NDC 66758-140
Requested package NDC 66758-140-81
11-digit product format 667580140
Labeler code 66758
Product ID 66758-140_b2817059-5c86-4f54-8a2f-c3ff9f12d9c5
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Potassium Bicarbonate
Dosage form TABLET, EFFERVESCENT
Route ORAL
Labeler Sandoz Inc.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2014-09-01
Marketing end 2022-01-31
Substance POTASSIUM BICARBONATE
Active strength 978 mg/1
Pharmacologic classes Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
NDC exclude flag No
Listing certified through 0000-00-00
Current FDA listing Historical FDA.report record 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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Potassium Bicarbonate ACTIVE INGREDIENT HM5Z15LEBN KLOR-CON/EF (POTASSIUM BICARBONATE) TABLET, EFFERVESCENT [SANDOZ INC.] 1 potassium cation ACTIVE MOIETY 295O53K152 KLOR-CON/EF (POTASSIUM BICARBONATE) TABLET, EFFERVESCENT [SANDOZ INC.] 1 cellulose, microcrystalline INACTIVE INGREDIENT OP1R32D61U KLOR-CON/EF (POTASSIUM BICARBONATE) TABLET, EFFERVESCENT [SANDOZ INC.] 1 citric acid monohydrate INACTIVE INGREDIENT 2968PHW8QP KLOR-CON/EF (POTASSIUM BICARBONATE) TABLET, EFFERVESCENT [SANDOZ INC.] 1 FD&C yellow no. 6 INACTIVE INGREDIENT H77VEI93A8 KLOR-CON/EF (POTASSIUM BICARBONATE) TABLET, EFFERVESCENT [SANDOZ INC.] 1 light mineral oil INACTIVE INGREDIENT N6K5787QVP KLOR-CON/EF (POTASSIUM BICARBONATE) TABLET, EFFERVESCENT [SANDOZ INC.] 1 saccharin INACTIVE INGREDIENT FST467XS7D KLOR-CON/EF (POTASSIUM BICARBONATE) TABLET, EFFERVESCENT [SANDOZ INC.] 1 talc INACTIVE INGREDIENT 7SEV7J4R1U KLOR-CON/EF (POTASSIUM BICARBONATE) TABLET, EFFERVESCENT [SANDOZ INC.] 1
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 66758-140-81 66758014081 100 POUCH in 1 CARTON (66758-140-81) > 1 TABLET, EFFERVESCENT in 1 POUCH (66758-140-94) 100 pouch 2014-09-01 2021-02-28 No No Current