NDC 72485-701-01 - Erythromycin Lactobionate

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 72485-701
Requested NDC: 72485-701-01
Package NDCs from labels: 72485-701-01, 72485-701-10
Manufacturer: Armas Pharmaceuticals Inc.
Effective date: 2026-07-09
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Erythromycin Lactobionate for Injection, USP	Armas Pharmaceuticals Inc.	2026-07-09	HUMAN PRESCRIPTION DRUG LABEL

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 4 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Erythromycin Lactobionate	ERYTHROMYCIN LACTOBIONATE	Piramal Critical Care Inc.	ee345752-0f0c-c69b-e053-2995a90a7dac	2026-08-16	Warnings, Adverse reactions	Exact identifier application number: ANDA216761 rxcui: 1668264 unii: 33H58I7GLQ
Erythromycin Lactobionate	ERYTHROMYCIN LACTOBIONATE	Armas Pharmaceuticals Inc.	ca65a48f-5fe6-4b31-8359-51dbc31f6d4e	2026-07-09	Warnings, Adverse reactions	Exact identifier application number: ANDA216761 ndc (package): 72485-701-10 ndc (package): 72485-701-01 ndc (product): 72485-701 ndc11 (package): 72485070101 rxcui: 1668264 spl id: 3430697d-5de8-4faf-994f-619aa4a2eea3 spl set id: ca65a48f-5fe6-4b31-8359-51dbc31f6d4e unii: 33H58I7GLQ
Erythrocin Lactobionate	ERYTHROMYCIN LACTOBIONATE	Hospira, Inc.	a96c405f-bd70-4bb4-719e-ac6a79dcc213	2025-10-30	Warnings, Adverse reactions	Exact identifier rxcui: 1668264 unii: 33H58I7GLQ
erythromycin lactobionate	ERYTHROMYCIN LACTOBIONATE	Gland Pharma Limited	c6f9565b-6d9d-40e3-87f8-9f38ede9173a	2024-11-20	Warnings, Adverse reactions	Exact identifier application number: ANDA216761 rxcui: 1668264 unii: 33H58I7GLQ

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.