Paroxetine

Product NDC: 13107-154
11-digit product format: 131070154
Labeler code: 13107
Product ID: 13107-154_c399d3cd-13a5-4493-9a93-c4bf5e2532fc
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Paroxetine
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Aurolife Pharma LLC
Application: ANDA078406
Marketing category: ANDA
Marketing start: 2009-12-03
Substance: PAROXETINE HYDROCHLORIDE HEMIHYDRATE
Active strength: 10 mg/1
Pharmacologic classes: Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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

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	TE codes	Approval date
A078406-001	PAROXETINE HYDROCHLORIDE	PAROXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL	AB	2007-07-25
A078406-002	PAROXETINE HYDROCHLORIDE	PAROXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL	AB	2007-07-25
A078406-003	PAROXETINE HYDROCHLORIDE	PAROXETINE HYDROCHLORIDE	EQ 30MG BASE	TABLET / ORAL	AB	2007-07-25
A078406-004	PAROXETINE HYDROCHLORIDE	PAROXETINE HYDROCHLORIDE	EQ 40MG BASE	TABLET / ORAL	AB	2007-07-25

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 4 matching rows.

Application-product, TE code table
Application-product	TE code
A078406-001	AB
A078406-002	AB
A078406-003	AB
A078406-004	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 1 of 5 · 164 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Product TE source text	Approval date	Source SHA-256
2026-02-19 14:30 UTC	2026-02	A078406-001	PAROXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL	AB	2007-07-25	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A078406-002	PAROXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL	AB	2007-07-25	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A078406-003	PAROXETINE HYDROCHLORIDE	EQ 30MG BASE	TABLET / ORAL	AB	2007-07-25	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A078406-004	PAROXETINE HYDROCHLORIDE	EQ 40MG BASE	TABLET / ORAL	AB	2007-07-25	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A078406-001	PAROXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL	AB	2007-07-25	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A078406-002	PAROXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL	AB	2007-07-25	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A078406-003	PAROXETINE HYDROCHLORIDE	EQ 30MG BASE	TABLET / ORAL	AB	2007-07-25	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A078406-004	PAROXETINE HYDROCHLORIDE	EQ 40MG BASE	TABLET / ORAL	AB	2007-07-25	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A078406-001	PAROXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL	AB	2007-07-25	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A078406-002	PAROXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL	AB	2007-07-25	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A078406-003	PAROXETINE HYDROCHLORIDE	EQ 30MG BASE	TABLET / ORAL	AB	2007-07-25	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A078406-004	PAROXETINE HYDROCHLORIDE	EQ 40MG BASE	TABLET / ORAL	AB	2007-07-25	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A078406-001	PAROXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL	AB	2007-07-25	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A078406-002	PAROXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL	AB	2007-07-25	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A078406-003	PAROXETINE HYDROCHLORIDE	EQ 30MG BASE	TABLET / ORAL	AB	2007-07-25	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A078406-004	PAROXETINE HYDROCHLORIDE	EQ 40MG BASE	TABLET / ORAL	AB	2007-07-25	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A078406-001	PAROXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL	AB	2007-07-25	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A078406-002	PAROXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL	AB	2007-07-25	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A078406-003	PAROXETINE HYDROCHLORIDE	EQ 30MG BASE	TABLET / ORAL	AB	2007-07-25	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A078406-004	PAROXETINE HYDROCHLORIDE	EQ 40MG BASE	TABLET / ORAL	AB	2007-07-25	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A078406-001	PAROXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL	AB	2007-07-25	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A078406-002	PAROXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL	AB	2007-07-25	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A078406-003	PAROXETINE HYDROCHLORIDE	EQ 30MG BASE	TABLET / ORAL	AB	2007-07-25	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A078406-004	PAROXETINE HYDROCHLORIDE	EQ 40MG BASE	TABLET / ORAL	AB	2007-07-25	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A078406-001	PAROXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL	AB	2007-07-25	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A078406-002	PAROXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL	AB	2007-07-25	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A078406-003	PAROXETINE HYDROCHLORIDE	EQ 30MG BASE	TABLET / ORAL	AB	2007-07-25	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A078406-004	PAROXETINE HYDROCHLORIDE	EQ 40MG BASE	TABLET / ORAL	AB	2007-07-25	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A078406-001	PAROXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL	AB	2007-07-25	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A078406-002	PAROXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL	AB	2007-07-25	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A078406-003	PAROXETINE HYDROCHLORIDE	EQ 30MG BASE	TABLET / ORAL	AB	2007-07-25	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A078406-004	PAROXETINE HYDROCHLORIDE	EQ 40MG BASE	TABLET / ORAL	AB	2007-07-25	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A078406-001	PAROXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL	AB	2007-07-25	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A078406-002	PAROXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL	AB	2007-07-25	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A078406-003	PAROXETINE HYDROCHLORIDE	EQ 30MG BASE	TABLET / ORAL	AB	2007-07-25	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A078406-004	PAROXETINE HYDROCHLORIDE	EQ 40MG BASE	TABLET / ORAL	AB	2007-07-25	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	A078406-001	PAROXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL	AB	2007-07-25	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	A078406-002	PAROXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL	AB	2007-07-25	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	A078406-003	PAROXETINE HYDROCHLORIDE	EQ 30MG BASE	TABLET / ORAL	AB	2007-07-25	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	A078406-004	PAROXETINE HYDROCHLORIDE	EQ 40MG BASE	TABLET / ORAL	AB	2007-07-25	`d06236e962d9…`

Observed Orange Book normalized TE history#

Normalized TE history page 1 of 5 · 164 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2026-02-19 14:30 UTC	2026-02	A078406-001	AB	1	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A078406-002	AB	1	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A078406-003	AB	1	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A078406-004	AB	1	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A078406-001	AB	1	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A078406-002	AB	1	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A078406-003	AB	1	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A078406-004	AB	1	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A078406-001	AB	1	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A078406-002	AB	1	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A078406-003	AB	1	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A078406-004	AB	1	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A078406-001	AB	1	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A078406-002	AB	1	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A078406-003	AB	1	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A078406-004	AB	1	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A078406-001	AB	1	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A078406-002	AB	1	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A078406-003	AB	1	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A078406-004	AB	1	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A078406-001	AB	1	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A078406-002	AB	1	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A078406-003	AB	1	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A078406-004	AB	1	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A078406-001	AB	1	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A078406-002	AB	1	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A078406-003	AB	1	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A078406-004	AB	1	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A078406-001	AB	1	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A078406-002	AB	1	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A078406-003	AB	1	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A078406-004	AB	1	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A078406-001	AB	1	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A078406-002	AB	1	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A078406-003	AB	1	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A078406-004	AB	1	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	A078406-001	AB	1	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	A078406-002	AB	1	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	A078406-003	AB	1	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	A078406-004	AB	1	`d06236e962d9…`

Additional Listing Data#

Finished product: Yes
Brand name base: Paroxetine
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
X2ELS050D8	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1738483	Internal RxNorm lookup
1738495	Internal RxNorm lookup
1738503	Internal RxNorm lookup
1738511	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
e1ea4019-bb66-403c-a3d5-6ae056a59116	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
2ace441e-5ed1-9a56-64e5-302d887093bd	Product name	7	20250107
ba9fc237-0e76-4ac8-d3c5-cdb4df9e9f7f	Product name	4	20220524
200c61bf-0879-1df7-72b7-b72a8497b114	Product name	3	20171006
b430fc19-562d-420b-53a2-64d42b938631	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
13107-154-01	Paroxetine	100 in 1 BOTTLE	TABLET, FILM COATED	100	15
13107-154-05	Paroxetine	500 in 1 BOTTLE	TABLET, FILM COATED	500	15
13107-154-30	Paroxetine	30 in 1 BOTTLE	TABLET, FILM COATED	30	15
13107-154-90	Paroxetine	90 in 1 BOTTLE	TABLET, FILM COATED	90	15
13107-154-99	Paroxetine	1000 in 1 BOTTLE	TABLET, FILM COATED	1000	15

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
13107-154-05	EA - Each	13107-154	483db895-5aff-4913-8356-0a5e119b7bf7	1	2012-07-24
13107-154-30	EA - Each	13107-154	6d1c640d-c9c7-472b-8953-42adfb41be28	1	2012-07-24
13107-154-90	EA - Each	13107-154	da008775-ee53-42dc-bd9a-9666f8ed004e	1	2014-10-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
PAROXETINE HYDROCHLORIDE HEMIHYDRATE	ACTIVE INGREDIENT	X2ELS050D8	PAROXETINE TABLET, FILM COATED [AUROLIFE PHARMA LLC]	8
PAROXETINE	ACTIVE MOIETY	41VRH5220H	PAROXETINE TABLET, FILM COATED [AUROLIFE PHARMA LLC]	8
ANHYDROUS DIBASIC CALCIUM PHOSPHATE	INACTIVE INGREDIENT	L11K75P92J	PAROXETINE TABLET, FILM COATED [AUROLIFE PHARMA LLC]	8
D&C RED NO. 30	INACTIVE INGREDIENT	2S42T2808B	PAROXETINE TABLET, FILM COATED [AUROLIFE PHARMA LLC]	8
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	PAROXETINE TABLET, FILM COATED [AUROLIFE PHARMA LLC]	8
DIBASIC CALCIUM PHOSPHATE DIHYDRATE	INACTIVE INGREDIENT	O7TSZ97GEP	PAROXETINE TABLET, FILM COATED [AUROLIFE PHARMA LLC]	8
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	PAROXETINE TABLET, FILM COATED [AUROLIFE PHARMA LLC]	8
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	PAROXETINE TABLET, FILM COATED [AUROLIFE PHARMA LLC]	8
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	PAROXETINE TABLET, FILM COATED [AUROLIFE PHARMA LLC]	8
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	PAROXETINE TABLET, FILM COATED [AUROLIFE PHARMA LLC]	8
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	PAROXETINE TABLET, FILM COATED [AUROLIFE PHARMA LLC]	8
POLYETHYLENE GLYCOL 400	INACTIVE INGREDIENT	B697894SGQ	PAROXETINE TABLET, FILM COATED [AUROLIFE PHARMA LLC]	8
POLYETHYLENE GLYCOL 6000	INACTIVE INGREDIENT	30IQX730WE	PAROXETINE TABLET, FILM COATED [AUROLIFE PHARMA LLC]	8
POLYSORBATE 80	INACTIVE INGREDIENT	6OZP39ZG8H	PAROXETINE TABLET, FILM COATED [AUROLIFE PHARMA LLC]	8
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	PAROXETINE TABLET, FILM COATED [AUROLIFE PHARMA LLC]	8
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	PAROXETINE TABLET, FILM COATED [AUROLIFE PHARMA LLC]	8
PAROXETINE HYDROCHLORIDE HEMIHYDRATE	ACTIVE INGREDIENT	X2ELS050D8	PAROXETINE TABLET, FILM COATED [PREFERRED PHARMACEUTICALS, INC.]	2
PAROXETINE	ACTIVE MOIETY	41VRH5220H	PAROXETINE TABLET, FILM COATED [PREFERRED PHARMACEUTICALS, INC.]	2
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS	INACTIVE INGREDIENT	L11K75P92J	PAROXETINE TABLET, FILM COATED [PREFERRED PHARMACEUTICALS, INC.]	2
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE	INACTIVE INGREDIENT	O7TSZ97GEP	PAROXETINE TABLET, FILM COATED [PREFERRED PHARMACEUTICALS, INC.]	2
D&C RED NO. 30	INACTIVE INGREDIENT	2S42T2808B	PAROXETINE TABLET, FILM COATED [PREFERRED PHARMACEUTICALS, INC.]	2
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	PAROXETINE TABLET, FILM COATED [PREFERRED PHARMACEUTICALS, INC.]	2
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	PAROXETINE TABLET, FILM COATED [PREFERRED PHARMACEUTICALS, INC.]	2
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	PAROXETINE TABLET, FILM COATED [PREFERRED PHARMACEUTICALS, INC.]	2
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	PAROXETINE TABLET, FILM COATED [PREFERRED PHARMACEUTICALS, INC.]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	PAROXETINE TABLET, FILM COATED [PREFERRED PHARMACEUTICALS, INC.]	2
POLYETHYLENE GLYCOL 400	INACTIVE INGREDIENT	B697894SGQ	PAROXETINE TABLET, FILM COATED [PREFERRED PHARMACEUTICALS, INC.]	2
POLYETHYLENE GLYCOL 6000	INACTIVE INGREDIENT	30IQX730WE	PAROXETINE TABLET, FILM COATED [PREFERRED PHARMACEUTICALS, INC.]	2
POLYSORBATE 80	INACTIVE INGREDIENT	6OZP39ZG8H	PAROXETINE TABLET, FILM COATED [PREFERRED PHARMACEUTICALS, INC.]	2
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	PAROXETINE TABLET, FILM COATED [PREFERRED PHARMACEUTICALS, INC.]	2
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	PAROXETINE TABLET, FILM COATED [PREFERRED PHARMACEUTICALS, INC.]	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
13107-154	PAROXETINE TABLET, FILM COATED [AUROLIFE PHARMA LLC]	14	Current NDC, Legacy NDC, 5 package rows	20250131_e1ea4019-bb66-403c-a3d5-6ae056a59116.zip

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 · 9 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Paroxetine	PAROXETINE	REMEDYREPACK INC.	f52ca1fc-fbf7-4b2b-9e74-975c310b8ce6	2026-07-27	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 078406 application number: ANDA078406
Paroxetine	PAROXETINE HYDROCHLORIDE	NorthStar Rx LLC	118320de-0632-4139-8b13-7428b41da0ac	2026-07-09	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 078406 application number: ANDA078406
Paroxetine	PAROXETINE	AvPAK	d9a5e0aa-e638-5d6e-75c2-20cb78fc4f43	2026-03-24	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 078406 application number: ANDA078406
Paroxetine	PAROXETINE	Aurolife Pharma LLC	e1ea4019-bb66-403c-a3d5-6ae056a59116	2025-06-07	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 078406 application number: ANDA078406 ndc (product): 13107-154
Paroxetine	PAROXETINE HYDROCHLORIDE	Aurobindo Pharma Limited	326e8ab0-6886-4749-9544-885b37070051	2025-05-15	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 078406 application number: ANDA078406
Paroxetine	PAROXETINE	NCS HealthCare of KY, LLC dba Vangard Labs	0a8a58c7-5008-4c65-ae0e-e4ee809b1807	2022-09-02	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 078406 application number: ANDA078406
Paroxetine	PAROXETINE	Proficient Rx LP	847118ec-c139-466c-834b-1ae0b6e1f791	2021-01-01	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 078406 application number: ANDA078406
Paroxetine	PAROXETINE	Aphena Pharma Solutions - Tennessee, LLC	662223ec-3b9b-4a85-9680-789522363a7b	2018-07-26	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 078406 application number: ANDA078406
Paroxetine	PAROXETINE	Aphena Pharma Solutions - Tennessee, LLC	30fd2fc4-f661-44c9-a9a9-9d0de0892e3c	2018-05-08	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 078406 application number: ANDA078406

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
X2ELS050D8	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	110429-35-1	PAROXETINE HYDROCHLORIDE HEMIHYDRATE
41VRH5220H	PAROXETINE	61869-08-7	Paroxetine

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1738483	PARoxetine HCl 10 MG Oral Tablet	PSN	e1ea4019-bb66-403c-a3d5-6ae056a59116	15
1738495	PARoxetine HCl 20 MG Oral Tablet	PSN	e1ea4019-bb66-403c-a3d5-6ae056a59116	15
1738503	PARoxetine HCl 30 MG Oral Tablet	PSN	e1ea4019-bb66-403c-a3d5-6ae056a59116	15
1738511	PARoxetine HCl 40 MG Oral Tablet	PSN	e1ea4019-bb66-403c-a3d5-6ae056a59116	15
1738483	paroxetine hydrochloride 10 MG Oral Tablet	SCD	e1ea4019-bb66-403c-a3d5-6ae056a59116	15
1738495	paroxetine hydrochloride 20 MG Oral Tablet	SCD	e1ea4019-bb66-403c-a3d5-6ae056a59116	15
1738503	paroxetine hydrochloride 30 MG Oral Tablet	SCD	e1ea4019-bb66-403c-a3d5-6ae056a59116	15
1738511	paroxetine hydrochloride 40 MG Oral Tablet	SCD	e1ea4019-bb66-403c-a3d5-6ae056a59116	15
1738483	PARoxetine HCl 10 MG Oral Tablet	PSN	ec4e1e42-713c-41ea-b62d-2f46b8b5be05	12
1738495	PARoxetine HCl 20 MG Oral Tablet	PSN	ec4e1e42-713c-41ea-b62d-2f46b8b5be05	12
1738483	paroxetine hydrochloride 10 MG Oral Tablet	SCD	ec4e1e42-713c-41ea-b62d-2f46b8b5be05	12
1738495	paroxetine hydrochloride 20 MG Oral Tablet	SCD	ec4e1e42-713c-41ea-b62d-2f46b8b5be05	12
1738483	PARoxetine HCl 10 MG Oral Tablet	PSN	f52ca1fc-fbf7-4b2b-9e74-975c310b8ce6	11
1738483	paroxetine hydrochloride 10 MG Oral Tablet	SCD	f52ca1fc-fbf7-4b2b-9e74-975c310b8ce6	11
1738483	PARoxetine HCl 10 MG Oral Tablet	PSN	d9a5e0aa-e638-5d6e-75c2-20cb78fc4f43	9
1738495	PARoxetine HCl 20 MG Oral Tablet	PSN	d9a5e0aa-e638-5d6e-75c2-20cb78fc4f43	9
1738503	PARoxetine HCl 30 MG Oral Tablet	PSN	d9a5e0aa-e638-5d6e-75c2-20cb78fc4f43	9
1738511	PARoxetine HCl 40 MG Oral Tablet	PSN	d9a5e0aa-e638-5d6e-75c2-20cb78fc4f43	9
1738483	paroxetine hydrochloride 10 MG Oral Tablet	SCD	d9a5e0aa-e638-5d6e-75c2-20cb78fc4f43	9
1738495	paroxetine hydrochloride 20 MG Oral Tablet	SCD	d9a5e0aa-e638-5d6e-75c2-20cb78fc4f43	9
1738503	paroxetine hydrochloride 30 MG Oral Tablet	SCD	d9a5e0aa-e638-5d6e-75c2-20cb78fc4f43	9
1738511	paroxetine hydrochloride 40 MG Oral Tablet	SCD	d9a5e0aa-e638-5d6e-75c2-20cb78fc4f43	9
1738483	PARoxetine HCl 10 MG Oral Tablet	PSN	0a8a58c7-5008-4c65-ae0e-e4ee809b1807	3
1738483	paroxetine hydrochloride 10 MG Oral Tablet	SCD	0a8a58c7-5008-4c65-ae0e-e4ee809b1807	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
13107-154-01	13107015401	100 TABLET, FILM COATED in 1 BOTTLE (13107-154-01)	2009-12-03	0000-00-00	No	No	Current
13107-154-05	13107015405	500 TABLET, FILM COATED in 1 BOTTLE (13107-154-05)	2009-12-03	0000-00-00	No	No	Current
13107-154-30	13107015430	30 TABLET, FILM COATED in 1 BOTTLE (13107-154-30)	2009-12-03	0000-00-00	No	No	Current
13107-154-90	13107015490	90 TABLET, FILM COATED in 1 BOTTLE (13107-154-90)	2009-12-03	0000-00-00	No	No	Current
13107-154-99	13107015499	1000 TABLET, FILM COATED in 1 BOTTLE (13107-154-99)	2009-12-03	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Paroxetine	REMEDYREPACK INC.	2026-07-27	HUMAN PRESCRIPTION DRUG LABEL	12
Paroxetine Tablets, USP	AvPAK	2026-03-24	HUMAN PRESCRIPTION DRUG LABEL	9
Paroxetine	Aurolife Pharma LLC \| Aurobindo Pharma Limited	2025-06-07	Human Prescription Drug Label	15
Paroxetine Tablets, USP Rx only	NCS HealthCare of KY, LLC dba Vangard Labs	2022-09-02	HUMAN PRESCRIPTION DRUG LABEL	3
Paroxetine Tablets, USP Rx only	A-S Medication Solutions	2021-06-10	Human Prescription Drug Label	12
Paroxetine Tablets, USP	Preferred Pharmaceuticals, Inc.	2017-12-06	HUMAN PRESCRIPTION DRUG LABEL	4