Application 020151
- Type
- NDA
- Sponsor
- WYETH PHARMS INC
Application Products#
| Product | Drug | Ingredient | Form | Strength | Reference drug | Reference standard |
|---|---|---|---|---|---|---|
| 001 | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | TABLET;ORAL | EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** | Yes | No |
| 002 | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | TABLET;ORAL | EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** | Yes | No |
| 003 | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | TABLET;ORAL | EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** | Yes | No |
| 004 | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | TABLET;ORAL | EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** | Yes | No |
| 005 | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | TABLET;ORAL | EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** | Yes | No |
| 006 | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | TABLET;ORAL | EQ 37.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** | Yes | No |
Orange Book products#
| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|---|---|---|---|---|---|---|
| N020151-001 | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | |
| N020151-002 | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | |
| N020151-003 | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | |
| N020151-004 | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | |
| N020151-005 | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | |
| N020151-006 | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | EQ 37.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 |
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.
| Captured | Edition | Application-product | Trade name | Strength | Dosage form / route | Product TE source text | RLD / RS | Approval date | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|
| 2026-09-14 22:38:34 | 2026-08 | N020151-001 | EFFEXOR | EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 84e616aacf4f… | |
| 2026-09-14 22:38:34 | 2026-08 | N020151-002 | EFFEXOR | EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 84e616aacf4f… | |
| 2026-09-14 22:38:34 | 2026-08 | N020151-003 | EFFEXOR | EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 84e616aacf4f… | |
| 2026-09-14 22:38:34 | 2026-08 | N020151-004 | EFFEXOR | EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 84e616aacf4f… | |
| 2026-09-14 22:38:34 | 2026-08 | N020151-005 | EFFEXOR | EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 84e616aacf4f… | |
| 2026-09-14 22:38:34 | 2026-08 | N020151-006 | EFFEXOR | EQ 37.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 84e616aacf4f… | |
| 2026-08-18 06:07:40 | 2026-07 | N020151-001 | EFFEXOR | EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | caaa826d4ba7… | |
| 2026-08-18 06:07:40 | 2026-07 | N020151-002 | EFFEXOR | EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | caaa826d4ba7… | |
| 2026-08-18 06:07:40 | 2026-07 | N020151-003 | EFFEXOR | EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | caaa826d4ba7… | |
| 2026-08-18 06:07:40 | 2026-07 | N020151-004 | EFFEXOR | EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | caaa826d4ba7… | |
| 2026-08-18 06:07:40 | 2026-07 | N020151-005 | EFFEXOR | EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | caaa826d4ba7… | |
| 2026-08-18 06:07:40 | 2026-07 | N020151-006 | EFFEXOR | EQ 37.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | caaa826d4ba7… | |
| 2026-02-19 14:30 UTC | 2026-02 | N020151-001 | EFFEXOR | EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 011fe1cb6892… | |
| 2026-02-19 14:30 UTC | 2026-02 | N020151-002 | EFFEXOR | EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 011fe1cb6892… | |
| 2026-02-19 14:30 UTC | 2026-02 | N020151-003 | EFFEXOR | EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 011fe1cb6892… | |
| 2026-02-19 14:30 UTC | 2026-02 | N020151-004 | EFFEXOR | EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 011fe1cb6892… | |
| 2026-02-19 14:30 UTC | 2026-02 | N020151-005 | EFFEXOR | EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 011fe1cb6892… | |
| 2026-02-19 14:30 UTC | 2026-02 | N020151-006 | EFFEXOR | EQ 37.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 011fe1cb6892… | |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | N020151-001 | EFFEXOR | EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 31067a03dcf5… | |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | N020151-002 | EFFEXOR | EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 31067a03dcf5… | |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | N020151-003 | EFFEXOR | EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 31067a03dcf5… | |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | N020151-004 | EFFEXOR | EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 31067a03dcf5… | |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | N020151-005 | EFFEXOR | EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 31067a03dcf5… | |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | N020151-006 | EFFEXOR | EQ 37.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 31067a03dcf5… | |
| 2025-08-23 18:47 UTC | 2025-08 | N020151-001 | EFFEXOR | EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 6a471c1ec25d… | |
| 2025-08-23 18:47 UTC | 2025-08 | N020151-002 | EFFEXOR | EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 6a471c1ec25d… | |
| 2025-08-23 18:47 UTC | 2025-08 | N020151-003 | EFFEXOR | EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 6a471c1ec25d… | |
| 2025-08-23 18:47 UTC | 2025-08 | N020151-004 | EFFEXOR | EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 6a471c1ec25d… | |
| 2025-08-23 18:47 UTC | 2025-08 | N020151-005 | EFFEXOR | EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 6a471c1ec25d… | |
| 2025-08-23 18:47 UTC | 2025-08 | N020151-006 | EFFEXOR | EQ 37.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | 6a471c1ec25d… | |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | N020151-001 | EFFEXOR | EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | fd3edfee7708… | |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | N020151-002 | EFFEXOR | EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | fd3edfee7708… | |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | N020151-003 | EFFEXOR | EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | fd3edfee7708… | |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | N020151-004 | EFFEXOR | EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | fd3edfee7708… | |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | N020151-005 | EFFEXOR | EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | fd3edfee7708… | |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | N020151-006 | EFFEXOR | EQ 37.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | fd3edfee7708… | |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | N020151-001 | EFFEXOR | EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | b8a1b40f171c… | |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | N020151-002 | EFFEXOR | EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | b8a1b40f171c… | |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | N020151-003 | EFFEXOR | EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | b8a1b40f171c… | |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | N020151-004 | EFFEXOR | EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET / ORAL | RLD | 1993-12-28 | b8a1b40f171c… |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | Preferred Pharmaceuticals Inc. | 6c1d0d4f-c8e2-4035-8f4e-7a46bfe3f059 | 2025-10-02 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | Preferred Pharmaceuticals Inc. | b055df74-51f9-401f-8cca-24269a0163df | 2025-10-02 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | Preferred Pharmaceuticals Inc. | 0c404290-2806-4756-bca3-2d639b400963 | 2025-10-02 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
| venlafaxine hydrochloride | VENLAFAXINE HYDROCHLORIDE | Preferred Pharmaceuticals Inc. | de6e30f8-c8ef-4016-b228-0f188645347b | 2025-10-02 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | Preferred Pharmaceuticals Inc. | 92b3f73d-d6ca-4d7d-9035-5700f527cb85 | 2025-10-02 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | Preferred Pharmaceuticals, Inc. | 653f3f95-98d0-4ce0-bf10-ac7938be690e | 2025-10-02 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | NuCare Pharmaceuticals, Inc. | 3cbe3e18-9a7e-aaa3-e063-6394a90abf92 | 2025-08-19 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
| VENLAFAXINE HYDROCHLORIDE | VENLAFAXINE HYDROCHLORIDE | Marlex Pharmaceuticals, Inc. | 3c2e188f-76aa-a022-e063-6294a90abfc9 | 2025-08-01 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | Trigen Laboratories, LLC | fdaed1c2-dd0a-4bf3-975a-86fe3e7f0c97 | 2025-07-31 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
| VENLAFAXINE HYDROCHLORIDE | VENLAFAXINE HYDROCHLORIDE | Alembic Pharmaceuticals Inc. | 5c943206-6df8-4fc5-ab1d-d34b9715182c | 2025-07-24 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | American Health Packaging | e05bdeb4-07a9-441e-901b-f2aea550db2b | 2025-06-24 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | ST. MARY'S MEDICAL PARK PHARMACY | 35d3148b-52f3-197c-e063-6294a90a44e3 | 2025-05-23 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
| venlafaxine hydrochloride | VENLAFAXINE HYDROCHLORIDE | Dr.Reddys Laboratories Inc | f5c21429-d5d0-9f93-a465-6e5e0e19ebdd | 2025-03-26 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | Preferred Pharmaceuticals Inc. | 15c77ad7-7edc-4c36-ba3f-3ef05dfb12dc | 2025-02-27 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | AvPAK | 2efde38c-250e-d1b9-e063-6394a90a1b74 | 2025-02-25 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | Advanced Rx of Tennessee, LLC | 2cf6e6ad-7d00-0db1-e063-6394a90ab1ec | 2025-01-31 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | Advanced Rx of Tennessee, LLC | 2c2bb0e6-5a73-ff57-e063-6294a90a88d3 | 2025-01-20 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
| Venlafaxine hydrochloride ER | VENLAFAXINE HYDROCHLORIDE | Advanced Rx Pharmacy of Tennessee, LLC | f8fd4381-52f2-d9c1-e053-6394a90a08e5 | 2024-12-31 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
| Venlafaxine Hydrochloride ER | VENLAFAXINE HYDROCHLORIDE | Advanced Rx Pharmacy of Tennessee, LLC | f7a9741b-2dd3-d8f3-e053-6294a90a4d73 | 2024-12-31 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
| Venlafaxine hydrochloride ER | VENLAFAXINE HYDROCHLORIDE | Advanced Rx Pharmacy of Tennessee, LLC | f89bcae0-e714-599a-e053-6294a90a2c3a | 2024-12-31 | Boxed warning, Warnings, Adverse reactions | VENLAFAXINE HYDROCHLORIDE |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Documents#
| Document | Submission type | Date |
|---|---|---|
| 46125 | SUPPL | 2016-12-09 |
| 2086 | SUPPL | 2012-12-19 |
| 2084 | SUPPL | 2012-12-19 |
| 2082 | SUPPL | 2012-12-19 |
| 2071 | SUPPL | 2012-12-19 |
| 34312 | SUPPL | 2012-12-13 |
| 34301 | SUPPL | 2012-12-13 |
| 12258 | SUPPL | 2012-12-13 |
| 12256 | SUPPL | 2012-12-13 |
| 2085 | SUPPL | 2012-05-09 |
| 12259 | SUPPL | 2012-05-07 |
| 2080 | SUPPL | 2010-01-19 |
| 21218 | SUPPL | 2010-01-14 |
| 2083 | SUPPL | 2010-01-14 |
| 34311 | SUPPL | 2010-01-08 |
| 12257 | SUPPL | 2010-01-08 |
| 34310 | SUPPL | 2009-11-13 |
| 12255 | SUPPL | 2009-02-04 |
| 2081 | SUPPL | 2009-02-03 |
| 34308 | SUPPL | 2008-11-20 |
| 21216 | SUPPL | 2008-05-28 |
| 34309 | SUPPL | 2008-02-14 |
| 21217 | SUPPL | 2008-02-14 |
| 2075 | SUPPL | 2008-02-05 |
| 20486 | SUPPL | 2007-11-19 |
| 20485 | SUPPL | 2007-11-19 |
| 20484 | SUPPL | 2007-11-19 |
| 34307 | SUPPL | 2007-09-26 |
| 34306 | SUPPL | 2007-09-26 |
| 2079 | SUPPL | 2007-09-25 |
| 2078 | SUPPL | 2007-09-25 |
| 34305 | SUPPL | 2007-08-02 |
| 21215 | SUPPL | 2007-08-02 |
| 12254 | SUPPL | 2007-08-02 |
| 41158 | SUPPL | 2007-07-06 |
| 20480 | SUPPL | 2007-07-06 |
| 41161 | SUPPL | 2007-07-05 |
| 41160 | SUPPL | 2007-07-05 |
| 41159 | SUPPL | 2007-07-05 |
| 41157 | SUPPL | 2007-07-05 |
| 20483 | SUPPL | 2007-07-05 |
| 20482 | SUPPL | 2007-07-05 |
| 20481 | SUPPL | 2007-07-05 |
| 34302 | SUPPL | 2007-02-21 |
| 2076 | SUPPL | 2007-02-12 |
| 34304 | SUPPL | 2006-10-23 |
| 2077 | SUPPL | 2006-10-23 |
| 21214 | SUPPL | 2006-09-20 |
| 34303 | SUPPL | 2006-09-15 |
| 2073 | SUPPL | 2006-03-01 |
| 21213 | SUPPL | 2006-01-20 |
| 2074 | SUPPL | 2006-01-20 |
| 23569 | ORIG | 2005-04-15 |
| 21212 | SUPPL | 2005-02-23 |
| 34299 | SUPPL | 2004-06-02 |
| 34300 | SUPPL | 2004-05-27 |
| 12253 | SUPPL | 2004-05-27 |
| 12252 | SUPPL | 2004-05-27 |
| 21211 | SUPPL | 2004-05-26 |
| 2072 | SUPPL | 2004-05-26 |
| 2070 | SUPPL | 2004-05-26 |
| 2068 | SUPPL | 2004-05-07 |
| 2069 | SUPPL | 2004-04-20 |
| 21210 | SUPPL | 2004-03-24 |
| 2067 | SUPPL | 2003-07-30 |
| 2066 | SUPPL | 2003-07-30 |
| 12251 | SUPPL | 2003-04-24 |
| 53536 | SUPPL | 1900-01-01 |
| 53535 | SUPPL | 1900-01-01 |
| 52225 | SUPPL | 1900-01-01 |
| 52223 | SUPPL | 1900-01-01 |
| 52222 | SUPPL | 1900-01-01 |