CHLORTHALIDONE

Product NDC
50090-3190
11-digit product format
500903190
Labeler code
50090
Product ID
50090-3190_83005019-d10f-4816-93ed-44d4cf7b4833
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
CHLORTHALIDONE
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA206904
Marketing category
ANDA
Marketing start
2017-05-17
Marketing end
0000-00-00
Substance
CHLORTHALIDONE
Active strength
25 mg/1
Pharmacologic classes
Thiazide-like Diuretic [EPC],Increased Diuresis [PE]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-3190-1EA - Each50090-31900f6b7ce2-ed8d-47cc-aae8-609068a3b65312019-05-02
50090-3190-2EA - Each50090-3190b0487567-d745-4ae1-be60-40e610537d0c12020-03-10

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-3190-050090319000100 TABLET in 1 BOTTLE (50090-3190-0) 100 tablet2019-09-300000-00-00NoNoCurrent
50090-3190-15009031900130 TABLET in 1 BOTTLE, PLASTIC (50090-3190-1) 30 tablet2017-11-160000-00-00NoNoCurrent
50090-3190-25009031900290 TABLET in 1 BOTTLE (50090-3190-2) 90 tablet2017-10-180000-00-00NoNoCurrent