NDC 10139-306-10 - Pamidronate Disodium

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: 10139-306
Requested NDC: 10139-306-10
Package NDCs from labels: 10139-306-10
Manufacturer: GeneraMedix, Inc.
Effective date: 2009-02-04
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Pamidronate Disodium - GeneraMedix, Inc.	GeneraMedix, Inc.	2009-02-04	HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10139-306-10	Pamidronate Disodium	10 mL in 1 VIAL	INJECTION, SOLUTION	10		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10139-306	PAMIDRONATE DISODIUM INJECTION, SOLUTION [GENERAMEDIX, INC.]	1	1 package rows	20090320_da574350-be6b-49f3-b2ef-64da06af9b9d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
PAMIDRONATE DISODIUM	ACTIVE INGREDIENT	8742T8ZQZA	PAMIDRONATE DISODIUM INJECTION, SOLUTION [GENERAMEDIX, INC.]	1
PAMIDRONIC ACID	ACTIVE MOIETY	OYY3447OMC	PAMIDRONATE DISODIUM INJECTION, SOLUTION [GENERAMEDIX, INC.]	1
MANNITOL	INACTIVE INGREDIENT	3OWL53L36A	PAMIDRONATE DISODIUM INJECTION, SOLUTION [GENERAMEDIX, INC.]	1
PHOSPHORIC ACID	INACTIVE INGREDIENT	E4GA8884NN	PAMIDRONATE DISODIUM INJECTION, SOLUTION [GENERAMEDIX, INC.]	1
SODIUM HYDROXIDE	INACTIVE INGREDIENT	55X04QC32I	PAMIDRONATE DISODIUM INJECTION, SOLUTION [GENERAMEDIX, INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	PAMIDRONATE DISODIUM INJECTION, SOLUTION [GENERAMEDIX, INC.]	1

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 · 3 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Pamidronate Disodium	PAMIDRONATE DISODIUM	Hospira, Inc.	9b6a9a3b-71c9-4dcb-b857-5d1de25c3a23	2026-05-14	Warnings, Adverse reactions	Exact identifier rxcui: 1737449 rxcui: 1737453
Pamidronate Disodium	PAMIDRONATE DISODIUM	Mylan Institutional LLC	c2ca033e-fa5f-4141-b702-11f8b4303da1	2025-12-15	Warnings, Adverse reactions	Exact identifier rxcui: 1737449 rxcui: 1737453
12F4C792-52EE-BC0D-FEBD-B393E2814E8F			da574350-be6b-49f3-b2ef-64da06af9b9d	2009-02-04	Warnings, Adverse reactions	Exact identifier spl id: 12F4C792-52EE-BC0D-FEBD-B393E2814E8F spl set id: da574350-be6b-49f3-b2ef-64da06af9b9d

Reported adverse events (FAERS/openFDA)#

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