FDA.reportPublic FDA data

Metronidazole

Product NDC
70518-2305
11-digit product format
705182305
Labeler code
70518
Product ID
70518-2305_49f24039-2b5d-6462-e063-6294a90a3711
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metronidazole
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA203458
Marketing category
ANDA
Marketing start
2019-09-09
Substance
METRONIDAZOLE
Active strength
500 mg/1
Pharmacologic classes
Nitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Metronidazole
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
METRONIDAZOLE500 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii140QMO216E
Rxcui311681

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
8ffb9b1d-3ed7-ba2e-677e-47d4d134fd55Product name520251024
7f6d14e0-4366-41bc-a4a9-b74c79a20e17Product name120250623
e6d321b0-0e5e-7da6-f043-92b6a91f00a1Product name520250515
e1aac33b-94ae-4ee9-905b-299f7263853bProduct name320250124
16642716-d28a-4f90-8dcb-3921cd8c8109Product name420240516
0be8e4ae-4d57-49f3-b3a9-e4728b4e8d15Product name120240313
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
a5070875-62bb-61e1-fd46-8f7054197a40Product name820180215
0add4de9-d152-3375-3390-1123dddc5e3dProduct name120140508
33ca0fcc-1011-92dc-50a9-a383683eed1eProduct name120140508
53f39d9f-cd3f-04e1-c668-d4580719d57dProduct name120140508
a804000f-b74f-0b5d-d17b-aa767c286ddbProduct name120140508
a91ea265-6e02-c08f-93c8-686d54180529Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-2305-0Metronidazole14 in 1 BOTTLE, PLASTICTABLET, FILM COATED1412
70518-2305-1Metronidazole4 in 1 BOTTLE, PLASTICTABLET, FILM COATED412
70518-2305-2Metronidazole4 in 1 BOXTABLET, FILM COATED412
70518-2305-3Metronidazole1 in 1 POUCHTABLET, FILM COATED112
70518-2305-4Metronidazole90 in 1 BOTTLE, PLASTICTABLET, FILM COATED9012

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-2305METRONIDAZOLE TABLET, FILM COATED [REMEDYREPACK INC.]9Current NDC, Legacy NDC, 5 package rows20250104_2f7d84d4-1085-4243-be88-442eecb85205.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311681metroNIDAZOLE 500 MG Oral TabletPSN2f7d84d4-1085-4243-be88-442eecb8520512
311681metronidazole 500 MG Oral TabletSCD2f7d84d4-1085-4243-be88-442eecb8520512

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
70518-2305-07051823050014 in 1 BOTTLE, PLASTICHistorical
70518-2305-1705182305014 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2305-1) 2022-01-310000-00-00NoNoCurrent
70518-2305-2705182305024 in 1 BOXHistorical
70518-2305-3705182305031 in 1 POUCHHistorical
70518-2305-47051823050490 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2305-4) 2025-09-13NoNoHistorical