FDA.reportPublic FDA data

Potassium Chloride

Product NDC
70436-153
11-digit product format
704360153
Labeler code
70436
Product ID
70436-153_3bc1f760-5a34-e736-e063-6394a90ab638
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Potassium Chloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Slate Run Pharmaceuticals, LLC
Application
ANDA212561
Marketing category
ANDA
Marketing start
2020-02-01
Substance
POTASSIUM CHLORIDE
Active strength
1500 mg/1
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
Listing certified through
2026-12-31
Current FDA listing
Yes

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9e37788c-b1bf-42ae-aac9-b60601606144Product name820260122
95250459-30e4-45c1-b08a-993044f49109Product name220250805
d9771140-739b-484b-ae64-b79528ff1211Product name320250801
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
1527ac37-808d-43be-a63e-74e1258dbe46Product name920250219
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9fcb7a91-de07-4f00-aabf-e4d6fda403d5Product name820230322
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
0ec3537a-6c9b-432a-896c-b9ea8723049aProduct name920200701
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
7916de40-e296-41f0-b811-6d0df1a33e2cProduct name920180627
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70436-153-01Potassium Chloride100 in 1 BOTTLETABLET, FILM COATED, EXTENDED RE10015
70436-153-02Potassium Chloride500 in 1 BOTTLETABLET, FILM COATED, EXTENDED RE50015

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70436-153-01EA - Each70436-1530d5dea67-ae82-4381-bb68-6d2397502c8812020-02-13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70436-153POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [SLATE RUN PHARMACEUTICALS, LLC]14Current NDC, Legacy NDC, 2 package rows20240621_94ae03cc-b620-0dbb-e053-2a95a90a922c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
628953potassium chloride 10 MEQ (750 MG) Extended Release Oral TabletPSN94ae03cc-b620-0dbb-e053-2a95a90a922c15
198116potassium chloride 20 MEQ Extended Release Oral TabletPSN94ae03cc-b620-0dbb-e053-2a95a90a922c15
628953potassium chloride 10 MEQ Extended Release Oral TabletSCD94ae03cc-b620-0dbb-e053-2a95a90a922c15
198116potassium chloride 20 MEQ Extended Release Oral TabletSCD94ae03cc-b620-0dbb-e053-2a95a90a922c15
628953K+ Chloride 10 MEQ Extended Release Oral TabletSY94ae03cc-b620-0dbb-e053-2a95a90a922c15
198116K+ Chloride 20 MEQ Extended Release Oral TabletSY94ae03cc-b620-0dbb-e053-2a95a90a922c15
628953Pot Chloride 10 MEQ Extended Release Oral TabletSY94ae03cc-b620-0dbb-e053-2a95a90a922c15
198116Pot Chloride 20 MEQ Extended Release Oral TabletSY94ae03cc-b620-0dbb-e053-2a95a90a922c15
198116potassium chloride 1500 MG (potassium 20 mEq) Extended Release Oral TabletSY94ae03cc-b620-0dbb-e053-2a95a90a922c15
198116potassium chloride 1500 MG Extended Release Oral TabletSY94ae03cc-b620-0dbb-e053-2a95a90a922c15
628953potassium chloride 750 MG (potassium 10 mEq) Extended Release Oral TabletSY94ae03cc-b620-0dbb-e053-2a95a90a922c15
628953potassium chloride 750 MG Extended Release Oral TabletSY94ae03cc-b620-0dbb-e053-2a95a90a922c15
198116potassium chloride 20 MEQ Extended Release Oral TabletPSN542e16b0-44db-490f-b44e-4c88a6e3d8b81
198116potassium chloride 20 MEQ Extended Release Oral TabletSCD542e16b0-44db-490f-b44e-4c88a6e3d8b81
198116K+ Chloride 20 MEQ Extended Release Oral TabletSY542e16b0-44db-490f-b44e-4c88a6e3d8b81
198116Pot Chloride 20 MEQ Extended Release Oral TabletSY542e16b0-44db-490f-b44e-4c88a6e3d8b81
198116potassium chloride 1500 MG (potassium 20 mEq) Extended Release Oral TabletSY542e16b0-44db-490f-b44e-4c88a6e3d8b81
198116potassium chloride 1500 MG Extended Release Oral TabletSY542e16b0-44db-490f-b44e-4c88a6e3d8b81

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
70436-153-0170436015301100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-153-01) 2020-02-010000-00-00NoNoCurrent
70436-153-0270436015302500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-153-02) 2020-02-010000-00-00NoNoCurrent