Application 019898

Type: NDA
Sponsor: BRISTOL MYERS SQUIBB

Application Products#

Product, Drug, Ingredient table
Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
002	PRAVACHOL	PRAVASTATIN SODIUM	TABLET;ORAL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No
003	PRAVACHOL	PRAVASTATIN SODIUM	TABLET;ORAL	20MG	Yes	No
004	PRAVACHOL	PRAVASTATIN SODIUM	TABLET;ORAL	40MG	Yes	No
008	PRAVACHOL	PRAVASTATIN SODIUM	TABLET;ORAL	80MG	Yes	Yes

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

Orange Book products#

Current product rows page 1 of 1 · 4 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	RLD / RS	Approval date
N019898-002	PRAVACHOL	PRAVASTATIN SODIUM	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31
N019898-003	PRAVACHOL	PRAVASTATIN SODIUM	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31
N019898-004	PRAVACHOL	PRAVASTATIN SODIUM	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1993-03-22
N019898-008	PRAVACHOL	PRAVASTATIN SODIUM	80MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	2001-12-18

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 5 · 172 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	N019898-002	PRAVACHOL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N019898-003	PRAVACHOL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N019898-004	PRAVACHOL	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1993-03-22	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N019898-008	PRAVACHOL	80MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	2001-12-18	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	N019898-002	PRAVACHOL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N019898-003	PRAVACHOL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N019898-004	PRAVACHOL	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1993-03-22	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N019898-008	PRAVACHOL	80MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	2001-12-18	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	N019898-002	PRAVACHOL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N019898-003	PRAVACHOL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N019898-004	PRAVACHOL	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1993-03-22	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N019898-008	PRAVACHOL	80MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	2001-12-18	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N019898-002	PRAVACHOL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N019898-003	PRAVACHOL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N019898-004	PRAVACHOL	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1993-03-22	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N019898-008	PRAVACHOL	80MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	2001-12-18	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	N019898-002	PRAVACHOL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N019898-003	PRAVACHOL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N019898-004	PRAVACHOL	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1993-03-22	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N019898-008	PRAVACHOL	80MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	2001-12-18	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N019898-002	PRAVACHOL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N019898-003	PRAVACHOL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N019898-004	PRAVACHOL	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1993-03-22	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N019898-008	PRAVACHOL	80MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	2001-12-18	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N019898-002	PRAVACHOL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N019898-003	PRAVACHOL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N019898-004	PRAVACHOL	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1993-03-22	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N019898-008	PRAVACHOL	80MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	2001-12-18	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N019898-002	PRAVACHOL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N019898-003	PRAVACHOL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N019898-004	PRAVACHOL	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1993-03-22	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N019898-008	PRAVACHOL	80MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	2001-12-18	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N019898-002	PRAVACHOL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N019898-003	PRAVACHOL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N019898-004	PRAVACHOL	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1993-03-22	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N019898-008	PRAVACHOL	80MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	2001-12-18	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N019898-002	PRAVACHOL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N019898-003	PRAVACHOL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-10-31	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N019898-004	PRAVACHOL	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1993-03-22	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N019898-008	PRAVACHOL	80MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	2001-12-18	`5bbf6a4d5a75…`

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2019-12-13 00:20 UTC	2019-12	N019898-003	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N019898-004	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N019898-008	AB	1	`74a2ff9319b5…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N019898-003	AB	1	`87673890dc5c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N019898-004	AB	1	`87673890dc5c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N019898-008	AB	1	`87673890dc5c…`
2021-03-12 10:30 UTC	2021-03	N019898-003	AB	1	`5aa47cf7b7d7…`
2021-03-12 10:30 UTC	2021-03	N019898-004	AB	1	`5aa47cf7b7d7…`
2021-03-12 10:30 UTC	2021-03	N019898-008	AB	1	`5aa47cf7b7d7…`
2020-12-22 03:56 UTC	2020-12	N019898-003	AB	1	`8869cabd3fbd…`
2020-12-22 03:56 UTC	2020-12	N019898-004	AB	1	`8869cabd3fbd…`
2020-12-22 03:56 UTC	2020-12	N019898-008	AB	1	`8869cabd3fbd…`
2020-11-12 02:37 UTC	2020-11	N019898-003	AB	1	`c0c555d07b60…`
2020-11-12 02:37 UTC	2020-11	N019898-004	AB	1	`c0c555d07b60…`
2020-11-12 02:37 UTC	2020-11	N019898-008	AB	1	`c0c555d07b60…`
2019-12-14 00:12 UTC	2019-12	N019898-003	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	N019898-004	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	N019898-008	AB	1	`3f01610625f2…`
2019-09-15 20:21 UTC	2019-09	N019898-003	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	N019898-004	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	N019898-008	AB	1	`b00525d2431f…`
2019-07-19 19:46 UTC	2019-07	N019898-003	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	N019898-004	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	N019898-008	AB	1	`ea99ee380514…`

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 5 of 7 · 121 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Pravastatin sodium	PRAVASTATIN SODIUM	Aurobindo Pharma Limited	c21d4797-d252-4073-891f-330484c5f643	2025-02-18	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM
Pravastatin sodium	PRAVASTATIN SODIUM	Aurobindo Pharma Limited	cf6f7031-33b9-40d3-bc87-32f1b6af98f2	2025-02-18	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM
PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	Aphena Pharma Solutions - Tennessee, LLC	2e5c8a1c-b36f-d124-e063-6394a90a6fb5	2025-02-17	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM
PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	Aphena Pharma Solutions - Tennessee, LLC	2e5cfae8-20b8-1fea-e063-6394a90a4e17	2025-02-17	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM
PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	Coupler LLC	2e0655ba-b1ba-789b-e063-6294a90a0a19	2025-02-13	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM
PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	Coupler LLC	2e07ad78-1059-e0ec-e063-6394a90a9bff	2025-02-13	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM
Pravastatin Sodium	PRAVASTATIN SODIUM	NuCare Pharmaceuticals, Inc.	2d40e473-f79a-e50e-e063-6294a90a4d9e	2025-02-03	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM
Pravastatin Sodium	PRAVASTATIN SODIUM	Chartwell RX, LLC	f87016fb-4c01-4279-8cf7-59819971ca15	2025-01-30	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM
PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	Bryant Ranch Prepack	7b900a28-f20e-49d5-98a9-5513fee0a901	2025-01-30	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM
PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	DIRECT RX	97178675-3691-2d93-e053-2995a90aa5c1	2025-01-17	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM
Pravastatin Sodium	PRAVASTATIN SODIUM	Quality Care Products, LLC	465dc828-966e-4bb4-b935-ef26583dd4e6	2024-12-19	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM
Pravastatin Sodium	PRAVASTATIN SODIUM	Lake Erie Medical DBA Quality Care Products LLC	e7194af1-6304-4e3e-88ab-0825706a3962	2024-12-11	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM
PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	NCS HealthCare of KY, LLC dba Vangard Labs	27ba8a69-b5aa-40eb-89f7-6bf2c1fcceae	2024-12-06	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM
Pravastatin Sodium	PRAVASTATIN SODIUM	A-S Medication Solutions	55f8cf43-bf8b-4729-9e5a-32fcc9696e02	2024-10-30	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM
PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	A-S Medication Solutions	7b4ef7a8-47e5-428f-91de-7307dcbb9167	2024-10-23	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM
PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	Bryant Ranch Prepack	6bb60d07-0787-4d5f-8a8c-1224d5b02b2b	2024-08-30	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM
PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	Bryant Ranch Prepack	06d85243-f9df-4984-b3d3-fcd8a7c554e9	2024-08-20	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM
PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	Bryant Ranch Prepack	01beb7e2-ba01-4f2f-8554-4a8ec0941c9f	2024-08-14	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM
PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	NuCare Pharmaceuticals, Inc.	54228087-7ab0-5561-e054-00144ff8d46c	2024-07-10	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM
PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	NuCare Pharmaceuticals,Inc.	548bdd9f-dcc6-28c7-e054-00144ff8d46c	2024-07-10	Warnings, Adverse reactions	Name fallback generic name: PRAVASTATIN SODIUM

Reported adverse events (FAERS/openFDA)#

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

NDC Listings For This Application#

NDC listings for this application page 1 of 1 · 8 matching rows.

NDC, Name, Nonproprietary name table
NDC	Name	Nonproprietary name	Labeler	Marketing category	Status
0003-5178	PRAVACHOL	PRAVASTATIN SODIUM	E.R. Squibb & Sons, L.L.C.	NDA	Current
0003-5178	PRAVACHOL	PRAVASTATIN SODIUM	E.R. Squibb & Sons, L.L.C.	NDA	Current
0003-5178	PRAVACHOL	PRAVASTATIN SODIUM	E.R. Squibb & Sons, L.L.C.	NDA	Current
0003-5194	PRAVACHOL	PRAVASTATIN SODIUM	E.R. Squibb & Sons, L.L.C.	NDA	Current
0003-5194	PRAVACHOL	PRAVASTATIN SODIUM	E.R. Squibb & Sons, L.L.C.	NDA	Current
0003-5194	PRAVACHOL	PRAVASTATIN SODIUM	E.R. Squibb & Sons, L.L.C.	NDA	Current
0003-5195	PRAVACHOL	PRAVASTATIN SODIUM	E.R. Squibb & Sons, L.L.C.	NDA	Current
0003-5195	PRAVACHOL	PRAVASTATIN SODIUM	E.R. Squibb & Sons, L.L.C.	NDA	Current

Documents#

Document, Submission type, Date table
Document	Submission type	Date
71221	SUPPL	2022-06-06
71183	SUPPL	2022-06-01
64726	SUPPL	2020-09-29
64698	SUPPL	2020-09-28
11829	SUPPL	2016-07-08
1788	SUPPL	2016-07-07
20414	SUPPL	2013-08-07
34081	SUPPL	2012-11-06
34080	SUPPL	2012-11-06
19811	SUPPL	2012-11-05
19810	SUPPL	2012-11-05
20415	SUPPL	2012-03-30
19809	SUPPL	2012-02-28
11828	SUPPL	2012-02-28
11827	SUPPL	2011-05-23
19808	SUPPL	2011-05-20
41085	SUPPL	2008-08-08
41087	SUPPL	2008-08-04
41086	SUPPL	2008-08-04
20413	SUPPL	2008-08-04
20412	SUPPL	2008-08-04
20411	SUPPL	2008-08-04
41090	SUPPL	2008-08-01
41080	SUPPL	2008-02-19
20409	SUPPL	2008-02-19
20408	SUPPL	2008-02-19
41089	SUPPL	2007-11-19
41088	SUPPL	2007-11-19
41077	SUPPL	2007-11-19
41081	SUPPL	2007-04-11
19807	SUPPL	2007-03-07
11826	SUPPL	2007-03-07
19806	SUPPL	2005-07-15
11825	SUPPL	2005-07-15
19805	SUPPL	2003-09-25
11824	SUPPL	2003-09-25
34079	SUPPL	2002-10-29
1787	SUPPL	2002-10-29
19804	SUPPL	2002-07-12
11823	SUPPL	2002-07-12
34078	SUPPL	2001-12-18
19803	SUPPL	2001-12-18
34077	SUPPL	2001-06-15
19802	SUPPL	2001-06-15
19801	SUPPL	2000-06-09
41082	SUPPL	2000-02-10
1784	SUPPL	2000-02-10
19800	SUPPL	2000-01-18
1783	SUPPL	2000-01-18
1782	SUPPL	2000-01-18
1781	SUPPL	2000-01-18
41084	SUPPL	1999-10-14
41083	SUPPL	1999-10-14
20410	SUPPL	1999-10-14
1786	SUPPL	1999-10-14
1785	SUPPL	1999-10-14
41079	SUPPL	1998-03-27
20407	SUPPL	1998-03-11
41078	SUPPL	1997-04-15