erythromycin lactobionate
Generic: erythromycin lactobionate
Labeler: nexus pharmaceuticals llcDrug Facts
Product Profile
Brand Name
erythromycin lactobionate
Generic Name
erythromycin lactobionate
Labeler
nexus pharmaceuticals llc
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
erythromycin lactobionate 500 mg/10mL
Manufacturer
Identifiers & Regulatory
Product NDC
14789-116
Product ID
14789-116_248996fd-c1f3-5b11-e063-6394a90ad2e3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215290
Listing Expiration
2026-12-31
Marketing Start
2021-08-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
14789116
Hyphenated Format
14789-116
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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 lactobionate (source: ndc)
Generic Name
erythromycin lactobionate (source: ndc)
Application Number
ANDA215290 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/10mL
Packaging
- 5 VIAL, GLASS in 1 BOX (14789-116-05) / 10 mL in 1 VIAL, GLASS (14789-116-07)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "248996fd-c1f3-5b11-e063-6394a90ad2e3", "openfda": {"unii": ["33H58I7GLQ"], "rxcui": ["1668264"], "spl_set_id": ["171b8b28-9da6-4bc6-85ea-f27fde5d5f10"], "manufacturer_name": ["Nexus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL, GLASS in 1 BOX (14789-116-05) / 10 mL in 1 VIAL, GLASS (14789-116-07)", "package_ndc": "14789-116-05", "marketing_start_date": "20210801"}], "brand_name": "Erythromycin Lactobionate", "product_id": "14789-116_248996fd-c1f3-5b11-e063-6394a90ad2e3", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Decreased Sebaceous Gland Activity [PE]", "Macrolide Antimicrobial [EPC]", "Macrolide [EPC]", "Macrolides [CS]"], "product_ndc": "14789-116", "generic_name": "Erythromycin Lactobionate", "labeler_name": "Nexus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Erythromycin Lactobionate", "active_ingredients": [{"name": "ERYTHROMYCIN LACTOBIONATE", "strength": "500 mg/10mL"}], "application_number": "ANDA215290", "marketing_category": "ANDA", "marketing_start_date": "20210801", "listing_expiration_date": "20261231"}