NITROFURANTOIN (monohydrate/macrocrystals)

Product NDC
76420-884
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nitrofurantoin (monohydrate/macrocrystals)
Dosage form
CAPSULE
Route
ORAL
Labeler
Asclemed USA, Inc.
Application
ANDA211013
Marketing category
ANDA
Substance
NITROFURANTOIN; NITROFURANTOIN MONOHYDRATE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
76420-884-001000 CAPSULE in 1 BOTTLE (76420-884-00) 2024-12-17NoHistorical
76420-884-01100 CAPSULE in 1 BOTTLE (76420-884-01) 2024-12-17NoHistorical
76420-884-077 CAPSULE in 1 BOTTLE (76420-884-07) 2024-12-17NoHistorical
76420-884-1010 CAPSULE in 1 BOTTLE (76420-884-10) 2025-01-09NoHistorical
76420-884-1212 CAPSULE in 1 BOTTLE (76420-884-12) 2024-12-17NoHistorical
76420-884-1414 CAPSULE in 1 BOTTLE (76420-884-14) 2024-12-17NoHistorical
76420-884-2020 CAPSULE in 1 BOTTLE (76420-884-20) 2024-12-17NoHistorical
76420-884-2828 CAPSULE in 1 BOTTLE (76420-884-28) 2024-12-17NoHistorical
76420-884-3030 CAPSULE in 1 BOTTLE (76420-884-30) 2024-12-17NoHistorical
76420-884-6060 CAPSULE in 1 BOTTLE (76420-884-60) 2024-12-17NoHistorical
76420-884-9090 CAPSULE in 1 BOTTLE (76420-884-90) 2024-12-17NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Nitrofurantoin Capsules, USP (monohydrate/macrocrystals)Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM2025-01-09HUMAN PRESCRIPTION DRUG LABEL2