FDA.reportPublic FDA data

Metronidazole

Product NDC
70518-0088
11-digit product format
705180088
Labeler code
70518
Product ID
70518-0088_47e248b3-5c6e-8131-e063-6394a90a9d8e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metronidazole
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA203458
Marketing category
ANDA
Marketing start
2016-12-28
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
70518-0088-0Metronidazole14 in 1 BLISTER PACKTABLET, FILM COATED1432
70518-0088-1Metronidazole28 in 1 BOTTLETABLET, FILM COATED2832
70518-0088-2Metronidazole14 in 1 BOTTLETABLET, FILM COATED1432
70518-0088-3Metronidazole4 in 1 BOTTLETABLET, FILM COATED432
70518-0088-4Metronidazole30 in 1 BLISTER PACKTABLET, FILM COATED3032
70518-0088-5Metronidazole21 in 1 BOTTLE, PLASTICTABLET, FILM COATED2132
70518-0088-6Metronidazole30 in 1 BOTTLE, PLASTICTABLET, FILM COATED3032

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-0088METRONIDAZOLE TABLET, FILM COATED [REMEDYREPACK INC.]29Current NDC, Legacy NDC, 7 package rows20250529_3c0ebb00-a0ae-4f64-9bfc-de01193191e8.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311681metroNIDAZOLE 500 MG Oral TabletPSN3c0ebb00-a0ae-4f64-9bfc-de01193191e832
311681metronidazole 500 MG Oral TabletSCD3c0ebb00-a0ae-4f64-9bfc-de01193191e832

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
70518-0088-07051800880014 TABLET, FILM COATED in 1 BLISTER PACK (70518-0088-0) 2016-12-280000-00-00NoNoCurrent
70518-0088-17051800880128 TABLET, FILM COATED in 1 BOTTLE (70518-0088-1) 2016-12-290000-00-00NoNoCurrent
70518-0088-27051800880214 TABLET, FILM COATED in 1 BOTTLE (70518-0088-2) 2016-12-300000-00-00NoNoCurrent
70518-0088-3705180088034 TABLET, FILM COATED in 1 BOTTLE (70518-0088-3) 2016-12-300000-00-00NoNoCurrent
70518-0088-47051800880430 TABLET, FILM COATED in 1 BLISTER PACK (70518-0088-4) 2017-01-310000-00-00NoNoCurrent
70518-0088-57051800880521 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0088-5) 2019-05-13NoNoCurrent
70518-0088-67051800880630 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0088-6) 2019-09-160000-00-00NoNoCurrent