Application 007073

Type: NDA
Sponsor: PHARMACIA AND UPJOHN

Application Products#

Product, Drug, Ingredient table
Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
001	AZULFIDINE	SULFASALAZINE	TABLET;ORAL	500MG	Yes	Yes
002	AZULFIDINE EN-TABS	SULFASALAZINE	TABLET, DELAYED RELEASE;ORAL	500MG	Yes	Yes

Source provenance: Browse the complete Orange Book source catalog · source snapshot 44.

Orange Book products#

Current product rows page 1 of 1 · 2 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	TE codes	RLD / RS	Approval date
N007073-001	AZULFIDINE	SULFASALAZINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982
N007073-002	AZULFIDINE EN-TABS	SULFASALAZINE	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 2 matching rows.

Application-product, TE code table
Application-product	TE code
N007073-001	AB
N007073-002	AB

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 2 of 3 · 88 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Product TE source text	RLD / RS	Approval date	Source SHA-256
2019-12-13 00:20 UTC	2019-12	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`74a2ff9319b5…`
2022-03-09 01:35 UTC	2022-03	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`bb7c543d1eb4…`
2022-03-09 01:35 UTC	2022-03	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`bb7c543d1eb4…`
2021-12-28 21:50 UTC	2021-12	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`782e0a99824c…`
2021-12-28 21:50 UTC	2021-12	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`782e0a99824c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`87673890dc5c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`87673890dc5c…`
2021-03-12 10:30 UTC	2021-03	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`5aa47cf7b7d7…`
2021-03-12 10:30 UTC	2021-03	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`5aa47cf7b7d7…`
2020-12-22 03:56 UTC	2020-12	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`8869cabd3fbd…`
2020-12-22 03:56 UTC	2020-12	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`8869cabd3fbd…`
2020-11-12 02:37 UTC	2020-11	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`c0c555d07b60…`
2020-11-12 02:37 UTC	2020-11	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`c0c555d07b60…`
2019-12-14 00:12 UTC	2019-12	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`3f01610625f2…`
2019-09-15 20:21 UTC	2019-09	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`b00525d2431f…`
2019-07-19 19:46 UTC	2019-07	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`ea99ee380514…`
2024-03-16 18:09 UTC · 4 captures of this ZIP	2024-03	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`6a51e52b5d6a…`
2024-03-16 18:09 UTC · 4 captures of this ZIP	2024-03	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`6a51e52b5d6a…`
2024-02-18 07:12 UTC	2024-02	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`1c564ffb4f44…`
2024-02-18 07:12 UTC	2024-02	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`1c564ffb4f44…`
2023-12-20 04:57 UTC	2023-12	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`ea1830bbd6c7…`
2023-12-20 04:57 UTC	2023-12	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`ea1830bbd6c7…`
2023-11-28 05:40 UTC · 2 captures of this ZIP	2023-11	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`a72a2bbeb626…`
2023-11-28 05:40 UTC · 2 captures of this ZIP	2023-11	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`a72a2bbeb626…`
2023-10-25 00:34 UTC · 2 captures of this ZIP	2023-10	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`9b2671bbb829…`
2023-10-25 00:34 UTC · 2 captures of this ZIP	2023-10	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`9b2671bbb829…`
2023-07-15 15:27 UTC · 2 captures of this ZIP	2023-07	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`a67488948f0b…`
2023-07-15 15:27 UTC · 2 captures of this ZIP	2023-07	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`a67488948f0b…`
2023-06-13 01:57 UTC · 3 captures of this ZIP	2023-06	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`3f0d92c62455…`
2023-06-13 01:57 UTC · 3 captures of this ZIP	2023-06	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`3f0d92c62455…`
2023-05-13 08:27 UTC	2023-05	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`053a50430f4f…`
2023-05-13 08:27 UTC	2023-05	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`053a50430f4f…`
2023-01-26 05:58 UTC	2023-01	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`3bdfa0b2c4d7…`
2023-01-26 05:58 UTC	2023-01	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`3bdfa0b2c4d7…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	N007073-001	AZULFIDINE	500MG	TABLET / ORAL	AB	RLD, RS, Approved before 1982		`3a93d1ddd44b…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	N007073-002	AZULFIDINE EN-TABS	500MG	TABLET, DELAYED RELEASE / ORAL	AB	RLD, RS	1983-04-06	`3a93d1ddd44b…`

Observed Orange Book normalized TE history#

Normalized TE history page 1 of 3 · 88 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2026-10-15 13:18:30	2026-09	N007073-001	AB	1	`c2088c7a36db…`
2026-10-15 13:18:30	2026-09	N007073-002	AB	1	`c2088c7a36db…`
2026-09-14 22:38:34	2026-08	N007073-001	AB	1	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N007073-002	AB	1	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	N007073-001	AB	1	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N007073-002	AB	1	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	N007073-001	AB	1	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N007073-002	AB	1	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N007073-001	AB	1	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N007073-002	AB	1	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	N007073-001	AB	1	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N007073-002	AB	1	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N007073-001	AB	1	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N007073-002	AB	1	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N007073-001	AB	1	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N007073-002	AB	1	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N007073-001	AB	1	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N007073-002	AB	1	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N007073-001	AB	1	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N007073-002	AB	1	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N007073-001	AB	1	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N007073-002	AB	1	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	N007073-001	AB	1	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	N007073-002	AB	1	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	N007073-001	AB	1	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	N007073-002	AB	1	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	N007073-001	AB	1	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	N007073-002	AB	1	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	N007073-001	AB	1	`301d65b070ca…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	N007073-002	AB	1	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N007073-001	AB	1	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N007073-002	AB	1	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	N007073-001	AB	1	`8072bd15b7f6…`
2024-05-31 18:47 UTC	2024-05	N007073-002	AB	1	`8072bd15b7f6…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	N007073-001	AB	1	`5c6f7cd8ea54…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	N007073-002	AB	1	`5c6f7cd8ea54…`
2022-04-08 23:34 UTC	2022-04	N007073-001	AB	1	`5d02ea3f76ae…`
2022-04-08 23:34 UTC	2022-04	N007073-002	AB	1	`5d02ea3f76ae…`
2022-04-04 05:41 UTC	2022-04	N007073-001	AB	1	`4b0b4de00fa7…`
2022-04-04 05:41 UTC	2022-04	N007073-002	AB	1	`4b0b4de00fa7…`

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 1 of 1 · 7 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sulfasalazine	SULFASALAZINE	Mylan Pharmaceuticals Inc.	257cee60-b68f-4c2b-b57d-8e4d73d17e09	2026-08-25	Warnings, Adverse reactions	Exact identifier application applno (NDA): 007073 application number: NDA007073 ndc (product): 59762-0104
Sulfasalazine	SULFASALAZINE	Mylan Pharmaceuticals Inc.	48fbc535-a33a-45ee-85ff-9d1ec9b31d9c	2026-08-25	Warnings, Adverse reactions	Exact identifier application applno (NDA): 007073 application number: NDA007073 ndc (product): 59762-5000
Azulfidine	SULFASALAZINE	Pfizer Laboratories Div Pfizer Inc	ddbe69f3-bd55-45f3-a64f-f60226c744c4	2026-05-29	Warnings, Adverse reactions	Exact identifier application applno (NDA): 007073 application number: NDA007073 ndc (product): 0013-0101
Azulfidine EN-tabs	SULFASALAZINE	Pfizer Laboratories Div Pfizer Inc	b9ef541a-93c8-4428-ba45-398aa0b327d1	2026-05-29	Warnings, Adverse reactions	Exact identifier application applno (NDA): 007073 application number: NDA007073 ndc (product): 0013-0102
Sulfasalazine	SULFASALAZINE	A-S Medication Solutions	76b532a3-e7ca-4929-8c51-c0f66e0806a8	2025-04-08	Warnings, Adverse reactions	Exact identifier application applno (NDA): 007073 application number: NDA007073
Sulfasalazine	SULFASALAZINE	A-S Medication Solutions	32fd1726-ed81-4441-9594-3aecf2db1dbf	2025-04-08	Warnings, Adverse reactions	Exact identifier application applno (NDA): 007073 application number: NDA007073 ndc (product): 50090-0086
Sulfasalazine	SULFASALAZINE	Aphena Pharma Solutions - Tennessee, LLC	bf5137fe-60ed-4497-8521-eeb0a684fabf	2023-05-16	Warnings, Adverse reactions	Exact identifier application applno (NDA): 007073 application number: NDA007073

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 · 52 matching rows.

NDC, Name, Nonproprietary name table
NDC	Name	Nonproprietary name	Labeler	Marketing category	Status
0013-0101	Azulfidine	Sulfasalazine	Pfizer Laboratories Div Pfizer Inc	NDA	Current
0013-0101	Azulfidine	Sulfasalazine	Pfizer Laboratories Div Pfizer Inc	NDA	Current
0013-0101	Azulfidine	Sulfasalazine	Pharmacia and Upjohn Company LLC	NDA	Current
0013-0101	Azulfidine	Sulfasalazine	Pharmacia and Upjohn Comp	NDA	Current
0013-0101	Azulfidine	Sulfasalazine	Pharmacia & Upjohn Company LLC	NDA	Current
0013-0101	Azulfidine	Sulfasalazine	Pfizer Laboratories Div Pfizer Inc	NDA	Current
0013-0101	Azulfidine	Sulfasalazine	Pharmacia & Upjohn Company LLC	NDA	Current
0013-0101	Azulfidine	Sulfasalazine	Pharmacia and Upjohn Company LLC	NDA	Current
0013-0101	Azulfidine	Sulfasalazine	Pharmacia and Upjohn Company LLC	NDA	Current
0013-0102	Azulfidine	Sulfasalazine	Pharmacia & Upjohn Company LLC	NDA	Current
0013-0102	Azulfidine	Sulfasalazine	Pharmacia & Upjohn Company LLC	NDA	Current
0013-0102	Azulfidine	Sulfasalazine	Pharmacia and Upjohn Company LLC	NDA	Current
0013-0102	Azulfidine	Sulfasalazine	Pharmacia and Upjohn Company LLC	NDA	Current
0013-0102	Azulfidine	Sulfasalazine	Pharmacia and Upjohn Company LLC	NDA	Current
0013-0102	Azulfidine	Sulfasalazine	Pharmacia & Upjohn Company LLC	NDA	Current
0013-0102	Azulfidine	Sulfasalazine	Pharmacia and Upjohn Company LLC	NDA	Current
0013-0102	Azulfidine	Sulfasalazine	Pfizer Laboratories Div Pfizer Inc	NDA	Current
0013-0102	Azulfidine	Sulfasalazine	Pfizer Laboratories Div Pfizer Inc	NDA	Current
0013-0102	Azulfidine	Sulfasalazine	Pfizer Laboratories Div Pfizer Inc	NDA	Current
0013-0102	Azulfidine	Sulfasalazine	Pharmacia & Upjohn Company LLC	NDA	Current
0013-0102	Azulfidine	Sulfasalazine	Pharmacia and Upjohn Comp	NDA	Current
43353-495	Sulfasalazine	Sulfasalazine	Aphena Pharma Solutions - Tennessee, LLC	NDA AUTHORIZED GENERIC	Current
43353-495	Sulfasalazine	Sulfasalazine	Aphena Pharma Solutions - Tennessee, LLC	NDA AUTHORIZED GENERIC	Current
50090-0086	Sulfasalazine	Sulfasalazine	A-S Medication Solutions	NDA AUTHORIZED GENERIC	Current
50090-0086	Sulfasalazine	Sulfasalazine	A-S Medication Solutions	NDA AUTHORIZED GENERIC	Current
50090-0086	Sulfasalazine	Sulfasalazine	A-S Medication Solutions	NDA AUTHORIZED GENERIC	Current
50090-0086	Sulfasalazine	Sulfasalazine	A-S Medication Solutions	NDA AUTHORIZED	Current
59762-0104	Sulfasalazine	Sulfasalazine	Greenstone LLC	NDA AUTHORIZED GENERIC	Current
59762-0104	Sulfasalazine	Sulfasalazine	Greenstone LLC	NDA AUTHORIZED GENERIC	Current
59762-0104	Sulfasalazine	Sulfasalazine	Greenstone LLC	NDA AUTHORIZED GENERIC	Current
59762-0104	Sulfasalazine	Sulfasalazine	Greenstone LLC	NDA AUTHORIZED GENERIC	Current
59762-0104	Sulfasalazine	Sulfasalazine	Greenstone LLC	NDA AUTHORIZED	Current
59762-0104	Sulfasalazine	Sulfasalazine	Greenstone LLC	NDA AUTHORIZED GENERIC	Current
59762-0104	Sulfasalazine	Sulfasalazine	Greenstone LLC	NDA AUTHORIZED GENERIC	Current
59762-0104	Sulfasalazine	Sulfasalazine	Greenstone LLC	NDA AUTHORIZED GENERIC	Current
59762-0104	Sulfasalazine	Sulfasalazine	Greenstone LLC	NDA AUTHORIZED GENERIC	Current
59762-0104	Sulfasalazine	Sulfasalazine	Greenstone LLC	NDA AUTHORIZED GENERIC	Current
59762-5000	Sulfasalazine	Sulfasalazine	Greenstone LLC	NDA AUTHORIZED GENERIC	Current
59762-5000	Sulfasalazine	Sulfasalazine	Greenstone LLC	NDA AUTHORIZED GENERIC	Current
59762-5000	Sulfasalazine	Sulfasalazine	Greenstone LLC	NDA AUTHORIZED GENERIC	Current
59762-5000	Sulfasalazine	Sulfasalazine	Greenstone LLC	NDA AUTHORIZED GENERIC	Current
59762-5000	Sulfasalazine	Sulfasalazine	Greenstone LLC	NDA AUTHORIZED	Current
59762-5000	Sulfasalazine	Sulfasalazine	Greenstone LLC	NDA AUTHORIZED GENERIC	Current
59762-5000	Sulfasalazine	Sulfasalazine	Greenstone LLC	NDA AUTHORIZED GENERIC	Current
59762-5000	Sulfasalazine	Sulfasalazine	Greenstone LLC	NDA AUTHORIZED GENERIC	Current
59762-5000	Sulfasalazine	Sulfasalazine	Greenstone LLC	NDA AUTHORIZED GENERIC	Current
70518-1829	Sulfasalazine	Sulfasalazine	REMEDYREPACK INC.	NDA AUTHORIZED GENERIC	Current
70518-1829	Sulfasalazine	Sulfasalazine	REMEDYREPACK INC.	NDA AUTHORIZED GENERIC	Current
70518-1829	Sulfasalazine	Sulfasalazine	REMEDYREPACK INC.	NDA AUTHORIZED GENERIC	Current
70518-1829	Sulfasalazine	Sulfasalazine	REMEDYREPACK INC.	NDA AUTHORIZED GENERIC	Current
70518-1829	Sulfasalazine	Sulfasalazine	REMEDYREPACK INC.	NDA AUTHORIZED GENERIC	Current
70518-1829	Sulfasalazine	Sulfasalazine	REMEDYREPACK INC.	NDA AUTHORIZED GENERIC	Current

Documents#

Document, Submission type, Date table
Document	Submission type	Date
72662	SUPPL	2022-11-21
72633	SUPPL	2022-11-17
69210	SUPPL	2021-11-02
69203	SUPPL	2021-11-02
65956	SUPPL	2021-01-22
65944	SUPPL	2021-01-21
86	SUPPL	2014-03-06
10689	SUPPL	2014-03-05
32949	SUPPL	2013-07-23
34	SUPPL	2013-07-22
85	SUPPL	2012-12-18
32948	SUPPL	2012-12-13
32947	SUPPL	2009-10-21
84	SUPPL	2004-05-27
83	SUPPL	2004-05-27
32946	SUPPL	2003-05-07