Chlorothiazide

Product NDC
0378-0150
11-digit product format
003780150
Labeler code
0378
Product ID
0378-0150_4f2271f7-98bc-4b5c-acc6-ad65a717ac84
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
chlorothiazide
Dosage form
TABLET
Route
ORAL
Labeler
Mylan Pharmaceuticals Inc.
Application
ANDA084217
Marketing category
ANDA
Marketing start
1975-06-26
Marketing end
2020-12-31
Substance
CHLOROTHIAZIDE
Active strength
250 mg/1
Pharmacologic classes
Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0378-0150-01EA - Each0378-015097f9a40c-e351-4981-ab87-886c1af9e0e312012-07-24