Nizatidine

Product NDC
42806-299
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nizatidine
Dosage form
CAPSULE
Route
ORAL
Labeler
Epic Pharma, LLC
Application
ANDA076178
Marketing category
ANDA
Substance
NIZATIDINE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
42806-299-3030 CAPSULE in 1 BOTTLE (42806-299-30) 2024-10-25NoHistorical
42806-299-6060 CAPSULE in 1 BOTTLE (42806-299-60) 2024-10-25NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
NIZATIDINE CAPSULES, USPEpic Pharma, LLC2025-01-02HUMAN PRESCRIPTION DRUG LABEL1