NDC 0591-5778 - Atenolol

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: 0591-5778
Package NDCs from labels: 0591-5778-01
Manufacturer: Rebel Distributors Corp.
Effective date: 2009-06-01
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Atenolol Tablets, USP	Rebel Distributors Corp.	2009-06-01	HUMAN PRESCRIPTION DRUG LABEL
Atenolol Tablets USP Revised: April 2006 Rx only	Watson Laboratories, Inc.	2007-03-02	HUMAN PRESCRIPTION DRUG LABELING
Atenolol Tablets USP Rx only	Watson Laboratories, Inc.	2006-03-08	HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0591-5778-01	Atenolol	100 in 1 BOTTLE	TABLET	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0591-5778	ATENOLOL (ATENOLOL) TABLET [WATSON LABORATORIES, INC.]	1	1 package rows	20070309_A32ECCC4-16D1-47A5-9E61-261F5D38638C.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Atenolol	ACTIVE INGREDIENT	50VV3VW0TI	ATENOLOL (ATENOLOL) TABLET [WATSON LABORATORIES, INC.]	1
ATENOLOL	ACTIVE INGREDIENT	50VV3VW0TI	ATENOLOL TABLET [REBEL DISTRIBUTORS CORP.]	1
Atenolol	ACTIVE INGREDIENT	50VV3VW0TI	ATENOLOL (ATENOLOL) TABLET [WATSON LABORATORIES, INC.]	1
Atenolol	ACTIVE MOIETY	50VV3VW0TI	ATENOLOL (ATENOLOL) TABLET [WATSON LABORATORIES, INC.]	1
ATENOLOL	ACTIVE MOIETY	50VV3VW0TI	ATENOLOL TABLET [REBEL DISTRIBUTORS CORP.]	1
Atenolol	ACTIVE MOIETY	50VV3VW0TI	ATENOLOL (ATENOLOL) TABLET [WATSON LABORATORIES, INC.]	1
COLLOIDAL SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	ATENOLOL TABLET [REBEL DISTRIBUTORS CORP.]	1
MAGNESIUM CARBONATE	INACTIVE INGREDIENT	0E53J927NA	ATENOLOL TABLET [REBEL DISTRIBUTORS CORP.]	1
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	ATENOLOL (ATENOLOL) TABLET [WATSON LABORATORIES, INC.]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	ATENOLOL TABLET [REBEL DISTRIBUTORS CORP.]	1
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	ATENOLOL (ATENOLOL) TABLET [WATSON LABORATORIES, INC.]	1
microcrystalline cellulose	INACTIVE INGREDIENT		ATENOLOL (ATENOLOL) TABLET [WATSON LABORATORIES, INC.]	1
microcrystalline cellulose	INACTIVE INGREDIENT		ATENOLOL (ATENOLOL) TABLET [WATSON LABORATORIES, INC.]	1
povidone	INACTIVE INGREDIENT		ATENOLOL (ATENOLOL) TABLET [WATSON LABORATORIES, INC.]	1
povidone	INACTIVE INGREDIENT		ATENOLOL (ATENOLOL) TABLET [WATSON LABORATORIES, INC.]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	ATENOLOL TABLET [REBEL DISTRIBUTORS CORP.]	1
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	ATENOLOL TABLET [REBEL DISTRIBUTORS CORP.]	1
sodium starch glycolate	INACTIVE INGREDIENT		ATENOLOL (ATENOLOL) TABLET [WATSON LABORATORIES, INC.]	1
sodium starch glycolate	INACTIVE INGREDIENT		ATENOLOL (ATENOLOL) TABLET [WATSON LABORATORIES, INC.]	1
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	ATENOLOL TABLET [REBEL DISTRIBUTORS CORP.]	1
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	ATENOLOL TABLET [REBEL DISTRIBUTORS CORP.]	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 40 of 40 · 785 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Thyrotox	CHONDRUS CRISPUS, FUCUS VESICULOSUS, THYROIDINUM, BELLADONNA, CALCAREA CARBONICA, CONIUM MACULATUM, IODIUM, KALI CARBONICUM, PHOSPHORUS, PULSATILLA (VULGARIS), SILICEA	BioActive Nutritional, Inc.	e229a260-13f3-4136-b325-9a8954f8a327	2016-08-10	Warnings	Exact identifier unii: ETJ7Z6XBU4
Teething	ARNICA MONTANA, TRIFOLIUM PRATENSE, CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, CHAMOMILLA, KREOSOTUM, SILICEA	BioActive Nutritional, Inc.	f39c9feb-f567-43a2-a026-2a581aeeed9d	2016-07-27	Warnings	Exact identifier unii: ETJ7Z6XBU4
d3e90e8f-d3c9-4c73-975f-206a28e0b103			aae36822-9c1b-4600-81d6-da022d56c03e	2009-06-01	Boxed warning, Warnings, Adverse reactions	Exact identifier spl id: d3e90e8f-d3c9-4c73-975f-206a28e0b103 spl set id: aae36822-9c1b-4600-81d6-da022d56c03e
C2C3B3F1-D236-EC09-9934-C3F9BA96E04B			A32ECCC4-16D1-47A5-9E61-261F5D38638C	2007-03-02	Boxed warning, Warnings, Adverse reactions	Exact identifier spl id: C2C3B3F1-D236-EC09-9934-C3F9BA96E04B spl set id: A32ECCC4-16D1-47A5-9E61-261F5D38638C
D18BCF6D-2F2D-4F70-735B-4CAD05CE9AF4			A5C67C7A-0FFD-4C51-BADB-B5109D4D25B6	2006-03-08	Warnings, Adverse reactions	Exact identifier spl id: D18BCF6D-2F2D-4F70-735B-4CAD05CE9AF4 spl set id: A5C67C7A-0FFD-4C51-BADB-B5109D4D25B6

Reported adverse events (FAERS/openFDA)#

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