erythromycin

Generic: erythromycin

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name erythromycin
Generic Name erythromycin
Labeler zydus lifesciences limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

erythromycin 500 mg/1

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 70771-1549
Product ID 70771-1549_35a32479-429b-4e71-9c5c-1e8ddbdff5e7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212693
Listing Expiration 2026-12-31
Marketing Start 2023-06-30

Pharmacologic Class

Established (EPC)
macrolide [epc] macrolide antimicrobial [epc]
Chemical Structure
macrolides [cs]
Physiologic Effect
decreased sebaceous gland activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707711549
Hyphenated Format 70771-1549

Supplemental Identifiers

RxCUI
197650 598006
UPC
0370771154913
UNII
63937KV33D
NUI
N0000009982 N0000175877 N0000175935 M0028311

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name erythromycin (source: ndc)
Generic Name erythromycin (source: ndc)
Application Number ANDA212693 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (70771-1549-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (70771-1549-3)
  • 500 TABLET, FILM COATED in 1 BOTTLE (70771-1549-5)
source: ndc

Packages (3)

70771-1549-1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1549-1) 70771-1549-3 30 TABLET, FILM COATED in 1 BOTTLE (70771-1549-3) 70771-1549-5 500 TABLET, FILM COATED in 1 BOTTLE (70771-1549-5)

Ingredients (1)

erythromycin (500 mg/1)

Linked Drug Pages (1)

Erythromycin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "35a32479-429b-4e71-9c5c-1e8ddbdff5e7", "openfda": {"nui": ["N0000009982", "N0000175877", "N0000175935", "M0028311"], "upc": ["0370771154913"], "unii": ["63937KV33D"], "rxcui": ["197650", "598006"], "spl_set_id": ["76608fdd-1248-4942-9518-fd8076244fa7"], "pharm_class_cs": ["Macrolides [CS]"], "pharm_class_pe": ["Decreased Sebaceous Gland Activity [PE]"], "pharm_class_epc": ["Macrolide [EPC]", "Macrolide Antimicrobial [EPC]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70771-1549-1)", "package_ndc": "70771-1549-1", "marketing_start_date": "20230630"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70771-1549-3)", "package_ndc": "70771-1549-3", "marketing_start_date": "20230630"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (70771-1549-5)", "package_ndc": "70771-1549-5", "marketing_start_date": "20230630"}], "brand_name": "Erythromycin", "product_id": "70771-1549_35a32479-429b-4e71-9c5c-1e8ddbdff5e7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Sebaceous Gland Activity [PE]", "Macrolide Antimicrobial [EPC]", "Macrolide [EPC]", "Macrolides [CS]"], "product_ndc": "70771-1549", "generic_name": "Erythromycin", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Erythromycin", "active_ingredients": [{"name": "ERYTHROMYCIN", "strength": "500 mg/1"}], "application_number": "ANDA212693", "marketing_category": "ANDA", "marketing_start_date": "20230630", "listing_expiration_date": "20261231"}