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INJECTABLE;INJECTION	EQ 250MG/50ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No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INJECTABLE;INJECTION	EQ 500MG/100ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No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INJECTABLE;INJECTION	EQ 750MG/150ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No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LEVAQUIN	LEVOFLOXACIN	EQ 500MG/20ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20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CONTAINER	LEVOFLOXACIN	EQ 250MG/50ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20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CONTAINER	LEVOFLOXACIN	EQ 500MG/100ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20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LEVAQUIN	LEVOFLOXACIN	EQ 750MG/30ML (EQ 25MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20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CONTAINER	LEVOFLOXACIN	EQ 750MG/150ML (EQ 5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE / INJECTION	RLD	1996-12-20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 2 of 4 · 77 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Levofloxacin	LEVOFLOXACIN	REMEDYREPACK INC.	b8ac5047-5203-42c4-886b-dd0b08a1786f	2026-01-12	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	REMEDYREPACK INC.	16d51c1c-4144-4be7-9356-98fcee621ecd	2026-01-09	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	Northwind Health Company, LLC	f2f090c2-3ee1-7689-e053-2995a90abe38	2026-01-01	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	Northwind Health Company, LLC	f780bb91-483a-d1a6-e053-6294a90ab74b	2026-01-01	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	Northwind Health Company, LLC	f33140d5-59ad-3379-e053-2995a90ae286	2026-01-01	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	BPI LABS LLC	b6d9740b-2f9d-4f1c-bc9b-4c2150b22f10	2025-12-26	Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
levofloxacin	LEVOFLOXACIN	Redpharm Drug	301ecffc-ecaf-01de-e063-6294a90a61b3	2025-12-23	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	ST. MARY'S MEDICAL PARK PHARMACY	46a3c619-b2a3-3f28-e063-6394a90a2309	2025-12-23	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	NuCare Pharmaceuticals,Inc.	c6027cde-b9fe-e593-e053-2995a90ac2c1	2025-12-19	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	Hospira, Inc	5a1534af-aa1c-4f1d-ba9f-9415b14e1af2	2025-11-04	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	VERITYRX, LLC	427a2077-5dbb-3c5e-e063-6294a90a0839	2025-10-31	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	PD-Rx Pharmaceuticals, Inc.	814450ae-439e-4a5d-8c60-9b21b6f14be5	2025-10-15	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	PD-Rx Pharmaceuticals, Inc.	b1a4aabb-42af-4133-8e82-0c7ec8fa79c3	2025-10-09	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	PD-Rx Pharmaceuticals, Inc.	b8defac4-9deb-433b-928e-0ef4ee0123a2	2025-10-02	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
levofloxacin	LEVOFLOXACIN	Bryant Ranch Prepack	cbd5153f-fada-4682-b858-dc3b6e3173cc	2025-09-29	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	Lannett Company, Inc.	362fb864-3afb-4841-a7c4-b64b1346aba0	2025-09-01	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	A-S Medication Solutions	1538ec66-f385-401e-8cfb-d794691e7176	2025-07-31	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	Proficient Rx LP	64141d0d-0347-470f-a427-9925a2eb357e	2025-07-01	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
Levofloxacin	LEVOFLOXACIN	Redpharm Drug	0a0fd993-7bea-42d8-e063-6394a90a4e0e	2025-04-09	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: LEVOFLOXACIN
LEVOFLOXACIN	LEVOFLOXACIN	Advagen Pharma Limited	f2eb9444-333d-4b05-8cf3-2e6690a2bf99	2025-03-10	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