NDC 62332-676

CHLORTHALIDONE CHLORTHALIDONE

Chlorthalidone

CHLORTHALIDONE CHLORTHALIDONE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Alembic Pharmaceuticals Inc.. The primary component is Chlorthalidone.

Product ID62332-676_56256d08-66bc-4424-84d4-2db217e5f4d6
NDC62332-676
Product TypeHuman Prescription Drug
Proprietary NameCHLORTHALIDONE CHLORTHALIDONE
Generic NameChlorthalidone
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2022-08-29
Marketing CategoryANDA /
Application NumberANDA216262
Labeler NameAlembic Pharmaceuticals Inc.
Substance NameCHLORTHALIDONE
Active Ingredient Strength25 mg/1
Pharm ClassesIncreased Diuresis [PE], Thiazide-like Diuretic [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 62332-676-31

100 TABLET in 1 BOTTLE (62332-676-31)
Marketing Start Date2022-08-29
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "CHLORTHALIDONE CHLORTHALIDONE" or generic name "Chlorthalidone"

NDCBrand NameGeneric Name
0378-0213Chlorthalidonechlorthalidone
0378-0222Chlorthalidonechlorthalidone
0904-6900ChlorthalidoneChlorthalidone
14803-505ChlorthalidoneChlorthalidone
14803-506ChlorthalidoneChlorthalidone
16714-128ChlorthalidoneChlorthalidone
16714-129ChlorthalidoneChlorthalidone
16714-800ChlorthalidoneChlorthalidone
16714-801ChlorthalidoneChlorthalidone
21695-671Chlorthalidonechlorthalidone
27241-216ChlorthalidoneChlorthalidone
27241-217ChlorthalidoneChlorthalidone
29300-333ChlorthalidoneChlorthalidone
29300-334ChlorthalidoneChlorthalidone
43353-922Chlorthalidonechlorthalidone
43598-167CHLORTHALIDONECHLORTHALIDONE
43598-170CHLORTHALIDONECHLORTHALIDONE
43598-719CHLORTHALIDONECHLORTHALIDONE
43598-720CHLORTHALIDONECHLORTHALIDONE
46708-676CHLORTHALIDONECHLORTHALIDONE
46708-677CHLORTHALIDONECHLORTHALIDONE
50090-0144Chlorthalidonechlorthalidone
50090-0145Chlorthalidonechlorthalidone
50090-3161ChlorthalidoneChlorthalidone

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.