Erythromycin

Product NDC
70771-1549
11-digit product format
707711549
Labeler code
70771
Product ID
70771-1549_35a32479-429b-4e71-9c5c-1e8ddbdff5e7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Erythromycin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Zydus Lifesciences Limited
Application
ANDA212693
Marketing category
ANDA
Marketing start
2023-06-30
Substance
ERYTHROMYCIN
Active strength
500 mg/1
Pharmacologic classes
Decreased Sebaceous Gland Activity [PE], Macrolide Antimicrobial [EPC], Macrolide [EPC], Macrolides [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
63937KV33DERYTHROMYCIN114-07-8ERYTHROMYCIN

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
70771-1549-170771154901100 TABLET, FILM COATED in 1 BOTTLE (70771-1549-1) 2023-06-30NoNoHistorical
70771-1549-37077115490330 TABLET, FILM COATED in 1 BOTTLE (70771-1549-3) 2023-06-30NoNoHistorical
70771-1549-570771154905500 TABLET, FILM COATED in 1 BOTTLE (70771-1549-5) 2023-06-30NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Erytrhomycin Tablets, USPZydus Lifesciences Limited2023-06-21HUMAN PRESCRIPTION DRUG LABEL2