Solodyn

Product NDC: 99207-463
Requested package NDC: 99207-463-02
11-digit product format: 992070463
Labeler code: 99207
Product ID: 99207-463_a594be33-33ce-4304-a6fe-65a4eeda3f19
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: minocycline hydrochloride
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Route: ORAL
Labeler: Bausch Health US LLC
Application: NDA050808
Marketing category: NDA
Marketing start: 2009-07-23
Marketing end: 0000-00-00
Substance: MINOCYCLINE HYDROCHLORIDE
Active strength: 65 mg/1
Pharmacologic classes: Tetracycline-class Drug [EPC],Tetracyclines [CS]
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	99207-463	99207-463-02	D	Discontinued by firm		2026-08-11

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 12 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`

Source provenance: Browse the complete Orange Book source catalog · source snapshot 1.

Orange Book products#

Current product rows page 1 of 1 · 8 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	RLD / RS	Approval date
N050808-001	SOLODYN	MINOCYCLINE HYDROCHLORIDE	EQ 45MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2006-05-08
N050808-002	SOLODYN	MINOCYCLINE HYDROCHLORIDE	EQ 90MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2006-05-08
N050808-003	SOLODYN	MINOCYCLINE HYDROCHLORIDE	EQ 135MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2006-05-08
N050808-004	SOLODYN	MINOCYCLINE HYDROCHLORIDE	EQ 65MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2009-07-23
N050808-005	SOLODYN	MINOCYCLINE HYDROCHLORIDE	EQ 115MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2009-07-23
N050808-006	SOLODYN	MINOCYCLINE HYDROCHLORIDE	EQ 105MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2010-08-27
N050808-007	SOLODYN	MINOCYCLINE HYDROCHLORIDE	EQ 80MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2010-08-27
N050808-008	SOLODYN	MINOCYCLINE HYDROCHLORIDE	EQ 55MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2010-08-27

Orange Book patents#

Current patent rows page 1 of 1 · 12 matching rows.

Application-product, Patent, Expiration table
Application-product	Patent	Expiration	Use code	Coverage / status	Submission date
N050808-001	7919483	2027-03-07	U-1078
N050808-002	7919483	2027-03-07	U-1078
N050808-002	7541347	2027-04-02	U-917
N050808-002	7544373	2027-04-02		Drug product
N050808-003	7919483	2027-03-07	U-1078
N050808-004	7919483	2027-03-07	U-1078
N050808-004	9192615	2031-11-17		Drug product	2016-01-08
N050808-005	7919483	2027-03-07	U-1078
N050808-005	9192615	2031-11-17		Drug product	2016-01-08
N050808-006	7919483	2027-03-07	U-1078
N050808-007	7919483	2027-03-07	U-1078
N050808-008	7919483	2027-03-07	U-1078

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 9 · 328 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	RLD / RS	Approval date	Source SHA-256
2026-02-19 14:30 UTC	2026-02	N050808-001	SOLODYN	EQ 45MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2006-05-08	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N050808-002	SOLODYN	EQ 90MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2006-05-08	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N050808-003	SOLODYN	EQ 135MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2006-05-08	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N050808-004	SOLODYN	EQ 65MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2009-07-23	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N050808-005	SOLODYN	EQ 115MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2009-07-23	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N050808-006	SOLODYN	EQ 105MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2010-08-27	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N050808-007	SOLODYN	EQ 80MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2010-08-27	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N050808-008	SOLODYN	EQ 55MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2010-08-27	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-001	SOLODYN	EQ 45MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2006-05-08	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-002	SOLODYN	EQ 90MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2006-05-08	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-003	SOLODYN	EQ 135MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2006-05-08	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-004	SOLODYN	EQ 65MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2009-07-23	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-005	SOLODYN	EQ 115MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2009-07-23	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-006	SOLODYN	EQ 105MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2010-08-27	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-007	SOLODYN	EQ 80MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2010-08-27	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-008	SOLODYN	EQ 55MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2010-08-27	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	N050808-001	SOLODYN	EQ 45MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2006-05-08	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N050808-002	SOLODYN	EQ 90MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2006-05-08	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N050808-003	SOLODYN	EQ 135MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2006-05-08	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N050808-004	SOLODYN	EQ 65MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2009-07-23	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N050808-005	SOLODYN	EQ 115MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2009-07-23	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N050808-006	SOLODYN	EQ 105MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2010-08-27	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N050808-007	SOLODYN	EQ 80MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2010-08-27	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N050808-008	SOLODYN	EQ 55MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2010-08-27	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N050808-001	SOLODYN	EQ 45MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2006-05-08	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N050808-002	SOLODYN	EQ 90MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2006-05-08	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N050808-003	SOLODYN	EQ 135MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2006-05-08	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N050808-004	SOLODYN	EQ 65MG BASE	TABLET, EXTENDED RELEASE / ORAL	RLD	2009-07-23	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N050808-005	SOLODYN	EQ 115MG BASE	TABLET, EXTENDED RELEASE / ORAL	RLD	2009-07-23	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N050808-006	SOLODYN	EQ 105MG BASE	TABLET, EXTENDED RELEASE / ORAL	RLD	2010-08-27	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N050808-007	SOLODYN	EQ 80MG BASE	TABLET, EXTENDED RELEASE / ORAL	RLD	2010-08-27	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N050808-008	SOLODYN	EQ 55MG BASE	TABLET, EXTENDED RELEASE / ORAL	RLD	2010-08-27	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N050808-001	SOLODYN	EQ 45MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2006-05-08	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N050808-002	SOLODYN	EQ 90MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2006-05-08	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N050808-003	SOLODYN	EQ 135MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	2006-05-08	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N050808-004	SOLODYN	EQ 65MG BASE	TABLET, EXTENDED RELEASE / ORAL	RLD	2009-07-23	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N050808-005	SOLODYN	EQ 115MG BASE	TABLET, EXTENDED RELEASE / ORAL	RLD	2009-07-23	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N050808-006	SOLODYN	EQ 105MG BASE	TABLET, EXTENDED RELEASE / ORAL	RLD	2010-08-27	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N050808-007	SOLODYN	EQ 80MG BASE	TABLET, EXTENDED RELEASE / ORAL	RLD	2010-08-27	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N050808-008	SOLODYN	EQ 55MG BASE	TABLET, EXTENDED RELEASE / ORAL	RLD	2010-08-27	`b8a1b40f171c…`

Observed Orange Book normalized TE history#

Normalized TE history page 1 of 4 · 140 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N050808-004	AB	1	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N050808-005	AB	1	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N050808-006	AB	1	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N050808-007	AB	1	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N050808-008	AB	1	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	N050808-004	AB	1	`8072bd15b7f6…`
2024-05-31 18:47 UTC	2024-05	N050808-005	AB	1	`8072bd15b7f6…`
2024-05-31 18:47 UTC	2024-05	N050808-006	AB	1	`8072bd15b7f6…`
2024-05-31 18:47 UTC	2024-05	N050808-007	AB	1	`8072bd15b7f6…`
2024-05-31 18:47 UTC	2024-05	N050808-008	AB	1	`8072bd15b7f6…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	N050808-004	AB	1	`5c6f7cd8ea54…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	N050808-005	AB	1	`5c6f7cd8ea54…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	N050808-006	AB	1	`5c6f7cd8ea54…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	N050808-007	AB	1	`5c6f7cd8ea54…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	N050808-008	AB	1	`5c6f7cd8ea54…`
2022-04-08 23:34 UTC	2022-04	N050808-004	AB	1	`5d02ea3f76ae…`
2022-04-08 23:34 UTC	2022-04	N050808-005	AB	1	`5d02ea3f76ae…`
2022-04-08 23:34 UTC	2022-04	N050808-006	AB	1	`5d02ea3f76ae…`
2022-04-08 23:34 UTC	2022-04	N050808-007	AB	1	`5d02ea3f76ae…`
2022-04-08 23:34 UTC	2022-04	N050808-008	AB	1	`5d02ea3f76ae…`
2022-04-04 05:41 UTC	2022-04	N050808-004	AB	1	`4b0b4de00fa7…`
2022-04-04 05:41 UTC	2022-04	N050808-005	AB	1	`4b0b4de00fa7…`
2022-04-04 05:41 UTC	2022-04	N050808-006	AB	1	`4b0b4de00fa7…`
2022-04-04 05:41 UTC	2022-04	N050808-007	AB	1	`4b0b4de00fa7…`
2022-04-04 05:41 UTC	2022-04	N050808-008	AB	1	`4b0b4de00fa7…`
2019-12-13 00:20 UTC	2019-12	N050808-004	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N050808-005	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N050808-006	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N050808-007	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N050808-008	AB	1	`74a2ff9319b5…`
2022-03-09 01:35 UTC	2022-03	N050808-004	AB	1	`bb7c543d1eb4…`
2022-03-09 01:35 UTC	2022-03	N050808-005	AB	1	`bb7c543d1eb4…`
2022-03-09 01:35 UTC	2022-03	N050808-006	AB	1	`bb7c543d1eb4…`
2022-03-09 01:35 UTC	2022-03	N050808-007	AB	1	`bb7c543d1eb4…`
2022-03-09 01:35 UTC	2022-03	N050808-008	AB	1	`bb7c543d1eb4…`
2021-12-28 21:50 UTC	2021-12	N050808-004	AB	1	`782e0a99824c…`
2021-12-28 21:50 UTC	2021-12	N050808-005	AB	1	`782e0a99824c…`
2021-12-28 21:50 UTC	2021-12	N050808-006	AB	1	`782e0a99824c…`
2021-12-28 21:50 UTC	2021-12	N050808-007	AB	1	`782e0a99824c…`
2021-12-28 21:50 UTC	2021-12	N050808-008	AB	1	`782e0a99824c…`

Observed Orange Book patent history#

Patent history page 1 of 39 · 1,545 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Patent	Expiration	Use code	Coverage / status	Submission date	Source SHA-256
2026-02-19 14:30 UTC	2026-02	N050808-001	7919483	2027-03-07	U-1078			`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N050808-002	7919483	2027-03-07	U-1078			`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N050808-002	7541347	2027-04-02	U-917			`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N050808-002	7544373	2027-04-02		Drug product		`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N050808-003	7919483	2027-03-07	U-1078			`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N050808-004	7919483	2027-03-07	U-1078			`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N050808-004	9192615	2031-11-17		Drug product	2016-01-08	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N050808-005	7919483	2027-03-07	U-1078			`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N050808-005	9192615	2031-11-17		Drug product	2016-01-08	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N050808-006	7919483	2027-03-07	U-1078			`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N050808-007	7919483	2027-03-07	U-1078			`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N050808-008	7919483	2027-03-07	U-1078			`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-001	7790705	2025-06-24	U-1078			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-001	8252776	2025-06-24	U-124		2012-08-28	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-001	8268804	2025-06-24	U-1078		2012-10-09	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-001	7919483	2027-03-07	U-1078			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-002	7790705	2025-06-24	U-1078			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-002	8252776	2025-06-24	U-124			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-002	8268804	2025-06-24	U-1078			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-002	7919483	2027-03-07	U-1078			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-002	7541347	2027-04-02	U-917			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-002	7544373	2027-04-02		Drug product		`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-003	7790705	2025-06-24	U-1078			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-003	8252776	2025-06-24	U-124			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-003	8268804	2025-06-24	U-1078			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-003	7919483	2027-03-07	U-1078			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-004	7790705	2025-06-24	U-1078			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-004	8252776	2025-06-24	U-124			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-004	8268804	2025-06-24	U-1078			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-004	7919483	2027-03-07	U-1078			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-004	9192615	2031-11-17		Drug product	2016-01-08	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-005	7790705	2025-06-24	U-1078			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-005	8252776	2025-06-24	U-124			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-005	8268804	2025-06-24	U-1078			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-005	7919483	2027-03-07	U-1078			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-005	9192615	2031-11-17		Drug product	2016-01-08	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-006	7790705	2025-06-24	U-1078			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-006	8252776	2025-06-24	U-124			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-006	8268804	2025-06-24	U-1078			`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N050808-006	8722650	2025-06-24	U-1078			`31067a03dcf5…`

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
99207-463-30	EA - Each	99207-463	eb517d66-2dd2-45ff-b201-51c94c6c7d4e	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
minocycline hydrochloride	ACTIVE INGREDIENT	0020414E5U	SOLODYN (MINOCYCLINE HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [MEDICIS PHARMACEUTICAL CORP.]	19
minocycline	ACTIVE MOIETY	FYY3R43WGO	SOLODYN (MINOCYCLINE HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [MEDICIS PHARMACEUTICAL CORP.]	19
D&C Red No. 27	INACTIVE INGREDIENT	2LRS185U6K	SOLODYN (MINOCYCLINE HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [MEDICIS PHARMACEUTICAL CORP.]	19
D&C Yellow No. 10	INACTIVE INGREDIENT	35SW5USQ3G	SOLODYN (MINOCYCLINE HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [MEDICIS PHARMACEUTICAL CORP.]	19
FD&C Blue No. 1	INACTIVE INGREDIENT	H3R47K3TBD	SOLODYN (MINOCYCLINE HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [MEDICIS PHARMACEUTICAL CORP.]	19
FD&C Blue No. 2	INACTIVE INGREDIENT	L06K8R7DQK	SOLODYN (MINOCYCLINE HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [MEDICIS PHARMACEUTICAL CORP.]	19
FD&C Red No. 40	INACTIVE INGREDIENT	WZB9127XOA	SOLODYN (MINOCYCLINE HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [MEDICIS PHARMACEUTICAL CORP.]	19
FD&C Yellow No. 6	INACTIVE INGREDIENT	H77VEI93A8	SOLODYN (MINOCYCLINE HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [MEDICIS PHARMACEUTICAL CORP.]	19
ferric oxide red	INACTIVE INGREDIENT	1K09F3G675	SOLODYN (MINOCYCLINE HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [MEDICIS PHARMACEUTICAL CORP.]	19
ferric oxide yellow	INACTIVE INGREDIENT	EX438O2MRT	SOLODYN (MINOCYCLINE HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [MEDICIS PHARMACEUTICAL CORP.]	19
ferrosoferric oxide	INACTIVE INGREDIENT	XM0M87F357	SOLODYN (MINOCYCLINE HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [MEDICIS PHARMACEUTICAL CORP.]	19
HYPROMELLOSE 2910 (50 MPA.S)	INACTIVE INGREDIENT	1IVH67816N	SOLODYN (MINOCYCLINE HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [MEDICIS PHARMACEUTICAL CORP.]	19
lactose monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	SOLODYN (MINOCYCLINE HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [MEDICIS PHARMACEUTICAL CORP.]	19
polyethylene glycol 3350	INACTIVE INGREDIENT	G2M7P15E5P	SOLODYN (MINOCYCLINE HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [MEDICIS PHARMACEUTICAL CORP.]	19
titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	SOLODYN (MINOCYCLINE HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [MEDICIS PHARMACEUTICAL CORP.]	19
triacetin	INACTIVE INGREDIENT	XHX3C3X673	SOLODYN (MINOCYCLINE HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [MEDICIS PHARMACEUTICAL CORP.]	19

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
0020414E5U	MINOCYCLINE HYDROCHLORIDE	13614-98-7	MINOCYCLINE HYDROCHLORIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
99207-463-02	99207046302	10 BOTTLE in 1 CARTON (99207-463-02) > 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE	10 bottle	2009-07-23	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Solodyn	Bausch Health US LLC \| Alcami Carolinas Corporation	2017-09-12	HUMAN PRESCRIPTION DRUG LABEL	27