Application 020635

Type: NDA
Sponsor: JANSSEN PHARMS

Application Products#

Product, Drug, Ingredient table
Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
001	LEVAQUIN	LEVOFLOXACIN	INJECTABLE;INJECTION	EQ 500MG/20ML (EQ 25MG/ML)	Yes	No
002	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	LEVOFLOXACIN	INJECTABLE;INJECTION	EQ 250MG/50ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No
003	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	LEVOFLOXACIN	INJECTABLE;INJECTION	EQ 500MG/100ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No
004	LEVAQUIN	LEVOFLOXACIN	INJECTABLE;INJECTION	EQ 750MG/30ML (EQ 25MG/ML)	Yes	No
005	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	LEVOFLOXACIN	INJECTABLE;INJECTION	EQ 750MG/150ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 5 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	RLD / RS	Approval date
N020635-001	LEVAQUIN	LEVOFLOXACIN	EQ 500MG/20ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20
N020635-002	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	LEVOFLOXACIN	EQ 250MG/50ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20
N020635-003	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	LEVOFLOXACIN	EQ 500MG/100ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20
N020635-004	LEVAQUIN	LEVOFLOXACIN	EQ 750MG/30ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20
N020635-005	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	LEVOFLOXACIN	EQ 750MG/150ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 1 of 6 · 215 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	RLD / RS	Approval date	Source SHA-256
2026-09-14 22:38:34	2026-08	N020635-001	LEVAQUIN	EQ 500MG/20ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N020635-002	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 250MG/50ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N020635-003	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 500MG/100ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N020635-004	LEVAQUIN	EQ 750MG/30ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N020635-005	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 750MG/150ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	N020635-001	LEVAQUIN	EQ 500MG/20ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N020635-002	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 250MG/50ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N020635-003	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 500MG/100ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N020635-004	LEVAQUIN	EQ 750MG/30ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N020635-005	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 750MG/150ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	N020635-001	LEVAQUIN	EQ 500MG/20ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N020635-002	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 250MG/50ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N020635-003	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 500MG/100ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N020635-004	LEVAQUIN	EQ 750MG/30ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N020635-005	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 750MG/150ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020635-001	LEVAQUIN	EQ 500MG/20ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020635-002	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 250MG/50ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020635-003	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 500MG/100ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020635-004	LEVAQUIN	EQ 750MG/30ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020635-005	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 750MG/150ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	N020635-001	LEVAQUIN	EQ 500MG/20ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N020635-002	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 250MG/50ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N020635-003	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 500MG/100ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N020635-004	LEVAQUIN	EQ 750MG/30ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N020635-005	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 750MG/150ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020635-001	LEVAQUIN	EQ 500MG/20ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020635-002	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 250MG/50ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020635-003	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 500MG/100ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020635-004	LEVAQUIN	EQ 750MG/30ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020635-005	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 750MG/150ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020635-001	LEVAQUIN	EQ 500MG/20ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020635-002	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 250MG/50ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020635-003	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 500MG/100ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020635-004	LEVAQUIN	EQ 750MG/30ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020635-005	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 750MG/150ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020635-001	LEVAQUIN	EQ 500MG/20ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020635-002	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 250MG/50ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020635-003	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 500MG/100ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020635-004	LEVAQUIN	EQ 750MG/30ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020635-005	LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER	EQ 750MG/150ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20	`03ed91905a0d…`

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 3 of 4 · 77 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Levofloxacin	LEVOFLOXACIN	NuCare Pharmaceuticals,Inc.	05d179f5-b200-8597-e063-6394a90a10cc	2025-03-04	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	NuCare Pharmaceuticals,Inc.	80501b71-2f08-2ef5-e053-2991aa0a6e86	2025-02-06	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
levofloxacin	LEVOFLOXACIN	Coupler LLC	2cee61b7-be51-0fe5-e063-6294a90af9e3	2025-01-30	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
levofloxacin	LEVOFLOXACIN	Preferred Pharmaceuticals Inc	067e260c-dc47-4957-a9ff-5a79f17b4ca0	2025-01-23	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	DirectRx	dabedb15-5b55-3853-e053-2995a90aa44e	2025-01-21	Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	PD-Rx Pharmaceuticals, Inc.	d98cf024-51fa-45a1-b247-da55aba88ca0	2025-01-14	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	NuCare Pharmaceuticals,Inc.	8423b021-e09c-4f1c-e053-2991aa0afef6	2025-01-02	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	ADVANCED RX PHARMACY OF TENNESSEE, LLC	af4b7333-4f77-4ec9-e053-2a95a90a16d2	2024-12-31	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	Advanced Rx of Tennessee, LLC	afd5cb35-4232-f8b1-e053-2a95a90a8c5b	2024-12-31	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	Advanced Rx of Tennessee, LLC	b001d60e-b8fb-54ff-e053-2a95a90a2970	2024-12-31	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	A-S Medication Solutions	bdc8b2cc-a914-4613-ac7c-e8dfe91dea13	2024-09-29	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	Golden State Medical Supply, Inc.	bfe280be-0789-69fa-e053-2a95a90a0e13	2024-09-16	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	Bryant Ranch Prepack	171ab6c6-8eb5-4716-926f-cee52b7d0968	2024-09-05	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
LEVOFLOXACIN	LEVOFLOXACIN	Gland Pharma Limited	ba69722b-d7f2-4519-8a63-9ee91294c499	2024-09-05	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	Bryant Ranch Prepack	54a02488-586d-4c4e-8a35-68a067bdd6e3	2024-08-26	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
levofloxacin	LEVOFLOXACIN	Bryant Ranch Prepack	b7a614b0-f604-48e1-9919-21da8f939d93	2024-08-26	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	Bryant Ranch Prepack	804ec547-5b89-4fd0-89b3-7445543e563e	2024-08-20	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
levofloxacin	LEVOFLOXACIN	Zydus Lifesciences Limited	ffa121b8-388f-4d7b-af48-d4aa8d9b5961	2024-08-16		Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	Camber Pharmaceuticals, Inc.	b43e9b51-568c-4d84-bbd1-d237120056c4	2024-08-14	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	NuCare Pharmaceuticals, Inc.	4a405103-41e8-6a1f-e054-00144ff8d46c	2024-07-19	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN

Reported adverse events (FAERS/openFDA)#

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

Documents#

Document, Submission type, Date table
Document	Submission type	Date
47162	SUPPL	2017-02-10
47150	SUPPL	2017-02-09
35039	SUPPL	2016-07-26
2959	SUPPL	2016-07-26
41511	SUPPL	2015-03-11
35038	SUPPL	2014-05-28
25402	SUPPL	2014-05-28
2958	SUPPL	2013-08-16
35037	SUPPL	2013-08-15
41512	SUPPL	2012-06-22
20791	SUPPL	2012-06-22
25399	SUPPL	2012-05-01
35035	SUPPL	2012-04-30
25401	SUPPL	2011-10-13
25400	SUPPL	2011-10-13
35036	SUPPL	2011-10-12
12901	SUPPL	2011-10-12
35034	SUPPL	2011-06-14
2957	SUPPL	2011-06-14
35033	SUPPL	2011-03-04
2956	SUPPL	2011-03-03
23172	ORIG	2009-11-19
35032	SUPPL	2009-05-11
25398	SUPPL	2009-05-05
2955	SUPPL	2009-03-13
12900	SUPPL	2008-10-08
25397	SUPPL	2008-10-07
41510	SUPPL	2008-08-01
41509	SUPPL	2008-08-01
24178	SUPPL	2008-07-16
12899	SUPPL	2008-06-05
2952	SUPPL	2008-05-08
25396	SUPPL	2008-04-18
2954	SUPPL	2008-01-09
12898	SUPPL	2007-12-14
35031	SUPPL	2007-11-19
35030	SUPPL	2007-11-19
25395	SUPPL	2007-11-19
2953	SUPPL	2007-11-19
2951	SUPPL	2007-09-25
2950	SUPPL	2007-09-25
35028	SUPPL	2007-09-19
35026	SUPPL	2007-09-19
25394	SUPPL	2007-07-05
35029	SUPPL	2007-06-27
35027	SUPPL	2007-06-04
25392	SUPPL	2007-06-04
25393	SUPPL	2007-05-16
12897	SUPPL	2007-05-16
12896	SUPPL	2006-06-28
2949	SUPPL	2006-06-28
12895	SUPPL	2006-01-27
35025	SUPPL	2005-08-08
25391	SUPPL	2005-08-08
20790	SUPPL	2005-06-27
20789	SUPPL	2005-06-27
20788	SUPPL	2005-06-27
35023	SUPPL	2004-12-03
25390	SUPPL	2004-12-02
35024	SUPPL	2004-11-08
2948	SUPPL	2004-11-08
12894	SUPPL	2004-09-15
12893	SUPPL	2004-09-15
2947	SUPPL	2004-09-15
2946	SUPPL	2004-09-15
41508	SUPPL	2004-09-09
20787	SUPPL	2004-09-09
2945	SUPPL	2004-07-21
35018	SUPPL	2004-06-08
12892	SUPPL	2004-04-05
25389	SUPPL	2004-03-10
2944	SUPPL	2003-12-04
35022	SUPPL	2003-06-08
2943	SUPPL	2003-06-08
2942	SUPPL	2002-10-30
35021	SUPPL	2001-12-18
35020	SUPPL	2001-12-18
35019	SUPPL	2001-12-18
25388	SUPPL	2001-12-18
25387	SUPPL	2001-12-18
25386	SUPPL	2001-12-18
25385	SUPPL	2000-09-08
12891	SUPPL	2000-09-08
25384	SUPPL	2000-02-02
20786	SUPPL	1999-07-02
2941	SUPPL	1998-12-17
20785	ORIG	1997-12-11
66975	SUPPL	1900-01-01
66974	SUPPL	1900-01-01
52016	SUPPL	1900-01-01
52015	SUPPL	1900-01-01
52010	SUPPL	1900-01-01
52007	SUPPL	1900-01-01
52004	SUPPL	1900-01-01