NDC 33342-150-01 - IBANDRONATE SODIUM

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: 33342-150
Requested NDC: 33342-150-01
Package NDCs from labels: 33342-150-52, 33342-150-01, 33342-150-53
Manufacturer: Macleods Pharmaceuticals Limited
Effective date: 2026-01-19
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
IBANDRONATE SODIUM - Macleods Pharmaceuticals Limited	Macleods Pharmaceuticals Limited	2026-01-19	Human Prescription Drug Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
33342-150-01	IBANDRONATE SODIUM	1 in 1 BLISTER PACK	TABLET, FILM COATED	1	12
33342-150-01	IBANDRONATE SODIUM	1 in 1 CARTON	TABLET, FILM COATED	1	12
33342-150-52	IBANDRONATE SODIUM	3 in 1 BLISTER PACK	TABLET, FILM COATED	3	12
33342-150-52	IBANDRONATE SODIUM	1 in 1 CARTON	TABLET, FILM COATED	1	12
33342-150-53	IBANDRONATE SODIUM	3 in 1 BOX	TABLET, FILM COATED	3	12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
33342-150	IBANDRONATE SODIUM TABLET, FILM COATED [MACLEODS PHARMACEUTICALS LIMITED]	5	Current NDC, Legacy NDC, 5 package rows	20220706_a5741ef6-0599-4657-8cda-2902ded4f680.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
33342-150-01	EA - Each	33342-150	5d7b7664-e003-4839-93d1-7434fd132632	1	2019-02-13
33342-150-52	EA - Each	33342-150	7736c70d-63ee-45ec-b80d-baf15b97438e	1	2025-07-08
33342-150-53	EA - Each	33342-150	b880f9f9-888e-4f46-a956-4697cbdeb47c	1	2019-02-13

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 133 of 133 · 2,643 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
TOTAL DEFENSE REPAIR BROAD SPECTRUM SPF 34 Sunscreen (Tinted)	OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE AND ZINC OXIDE	Allergan, Inc.	6a996e03-907f-4e6a-b232-0892b86956b0	2015-08-21	Warnings	Exact identifier unii: 15FIX9V2JP
Renewal Firming Day Broad Spectrum SPF 30	TITANIUM DIOXIDE, ZINC OXIDE	BURT'S BEES, INC.	18ceb5d8-4b76-6a54-e054-00144ff88e88	2015-06-18	Warnings	Exact identifier unii: 15FIX9V2JP
TiZO2	TITANIUM DIOXIDE, ZINC OXIDE	Fallien Cosmeceuticals, LTD.	30468afc-9616-4765-b046-12e97a0a7827	2010-12-20	Warnings	Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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