Fluoxetine

Product NDC: 0093-7188
11-digit product format: 000937188
Labeler code: 0093
Product ID: 0093-7188_36f18cc3-526a-4448-a4fb-803303acd103
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Fluoxetine
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Teva Pharmaceuticals USA, Inc.
Application: ANDA075872
Marketing category: ANDA
Marketing start: 2002-01-30
Marketing end: 2023-05-31
Substance: FLUOXETINE HYDROCHLORIDE
Active strength: 10 mg/1
Pharmacologic classes: Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
NDC exclude flag: No
Listing certified through: 0000-00-00
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 · 4 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	0093-7188		D	Discontinued by firm	2026-10-16
excluded package	package	0093-7188	0093-7188-01	D	Discontinued by firm	2026-10-16
excluded package	package	0093-7188	0093-7188-10	D	Discontinued by firm	2026-10-16
excluded package	package	0093-7188	0093-7188-56	D	Discontinued by firm	2026-10-16

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 · 48 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	0093-7188-56	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	0093-7188-01	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	0093-7188-10	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	0093-7188-56	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	0093-7188-01	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	0093-7188-10	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	0093-7188-56	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	0093-7188-01	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	0093-7188-10	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	0093-7188-56	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	0093-7188-01	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	0093-7188-10	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	0093-7188-56	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	0093-7188-01	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	0093-7188-10	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	0093-7188-56	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	0093-7188-01	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	0093-7188-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	0093-7188-56	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	0093-7188-01	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	0093-7188-10	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	0093-7188-56	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	0093-7188-01	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	0093-7188-10	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	0093-7188-56	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	0093-7188-01	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	0093-7188-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	0093-7188-56	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	0093-7188-01	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	0093-7188-10	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	0093-7188-56	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	0093-7188-01	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	0093-7188-10	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	0093-7188-56	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	0093-7188-01	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	0093-7188-10	`557ba5c1ecfa…`	`9c80585c8c6e…`

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
A075872-001	FLUOXETINE HYDROCHLORIDE	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL			2002-01-29
A075872-002	FLUOXETINE HYDROCHLORIDE	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL			2019-01-04

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 3 · 88 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
2026-10-15 13:18:30	2026-09	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL		2002-01-29	`c2088c7a36db…`
2026-10-15 13:18:30	2026-09	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL		2019-01-04	`c2088c7a36db…`
2026-09-14 22:38:34	2026-08	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL		2002-01-29	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL		2019-01-04	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL		2002-01-29	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL		2019-01-04	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL		2002-01-29	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL		2019-01-04	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL		2002-01-29	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL		2019-01-04	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL		2002-01-29	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL		2019-01-04	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL		2002-01-29	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL		2019-01-04	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL		2002-01-29	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL		2019-01-04	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL		2002-01-29	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL		2019-01-04	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL		2002-01-29	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL		2019-01-04	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL		2002-01-29	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL		2019-01-04	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL		2002-01-29	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL		2019-01-04	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL		2002-01-29	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL		2019-01-04	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL		2002-01-29	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL		2019-01-04	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL		2002-01-29	`301d65b070ca…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL		2019-01-04	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL		2002-01-29	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL		2019-01-04	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL		2002-01-29	`8072bd15b7f6…`
2024-05-31 18:47 UTC	2024-05	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL		2019-01-04	`8072bd15b7f6…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL	AB	2002-01-29	`5c6f7cd8ea54…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL	AB	2019-01-04	`5c6f7cd8ea54…`
2022-04-08 23:34 UTC	2022-04	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL	AB	2002-01-29	`5d02ea3f76ae…`
2022-04-08 23:34 UTC	2022-04	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL	AB	2019-01-04	`5d02ea3f76ae…`
2022-04-04 05:41 UTC	2022-04	A075872-001	FLUOXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET / ORAL	AB	2002-01-29	`4b0b4de00fa7…`
2022-04-04 05:41 UTC	2022-04	A075872-002	FLUOXETINE HYDROCHLORIDE	EQ 20MG BASE	TABLET / ORAL	AB	2019-01-04	`4b0b4de00fa7…`

Observed Orange Book normalized TE history#

Normalized TE history page 2 of 2 · 48 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	A075872-001	AB	1	`3a93d1ddd44b…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	A075872-002	AB	1	`3a93d1ddd44b…`
2022-10-28 04:53 UTC	2022-10	A075872-001	AB	1	`f41ea6bd6efb…`
2022-10-28 04:53 UTC	2022-10	A075872-002	AB	1	`f41ea6bd6efb…`
2022-09-29 23:25 UTC	2022-09	A075872-001	AB	1	`e64feba35796…`
2022-09-29 23:25 UTC	2022-09	A075872-002	AB	1	`e64feba35796…`
2022-07-09 03:26 UTC · 3 captures of this ZIP	2022-07	A075872-001	AB	1	`cb3db0bc1861…`
2022-07-09 03:26 UTC · 3 captures of this ZIP	2022-07	A075872-002	AB	1	`cb3db0bc1861…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0093-7188-01	EA - Each	0093-7188	d10fdd8f-1946-4e56-aff3-1e8fd614a4f0	1	2019-12-10
0093-7188-10	EA - Each	0093-7188	f181278c-f7d3-4377-91f1-877e3f208613	1	2012-07-24
0093-7188-56	EA - Each	0093-7188	d0e4dde8-5052-4731-a7ad-0bdf756b238b	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
FLUOXETINE HYDROCHLORIDE	ACTIVE INGREDIENT	I9W7N6B1KJ	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC]	9
FLUOXETINE	ACTIVE MOIETY	01K63SUP8D	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC]	9
ALUMINUM OXIDE	INACTIVE INGREDIENT	LMI26O6933	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC]	9
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC]	9
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC]	9
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC]	9
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC]	9
HYPROMELLOSE 2910 (5 MPA.S)	INACTIVE INGREDIENT	R75537T0T4	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC]	9
INDIGOTINDISULFONATE SODIUM	INACTIVE INGREDIENT	D3741U8K7L	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC]	9
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC]	9
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC]	9
POLYETHYLENE GLYCOL 6000	INACTIVE INGREDIENT	30IQX730WE	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC]	9
POLYETHYLENE GLYCOL 8000	INACTIVE INGREDIENT	Q662QK8M3B	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC]	9
POVIDONE K30	INACTIVE INGREDIENT	U725QWY32X	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC]	9
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC]	9
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC]	9
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC]	9
FLUOXETINE HYDROCHLORIDE	ACTIVE INGREDIENT	I9W7N6B1KJ	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [PROFICIENT RX LP]	1
FLUOXETINE	ACTIVE MOIETY	01K63SUP8D	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [PROFICIENT RX LP]	1
ALUMINUM OXIDE	INACTIVE INGREDIENT	LMI26O6933	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [PROFICIENT RX LP]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [PROFICIENT RX LP]	1
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [PROFICIENT RX LP]	1
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [PROFICIENT RX LP]	1
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [PROFICIENT RX LP]	1
HYPROMELLOSE 2910 (5 MPA.S)	INACTIVE INGREDIENT	R75537T0T4	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [PROFICIENT RX LP]	1
INDIGOTINDISULFONATE SODIUM	INACTIVE INGREDIENT	D3741U8K7L	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [PROFICIENT RX LP]	1
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [PROFICIENT RX LP]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [PROFICIENT RX LP]	1
POLYETHYLENE GLYCOL 6000	INACTIVE INGREDIENT	30IQX730WE	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [PROFICIENT RX LP]	1
POLYETHYLENE GLYCOL 8000	INACTIVE INGREDIENT	Q662QK8M3B	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [PROFICIENT RX LP]	1
POVIDONE K30	INACTIVE INGREDIENT	U725QWY32X	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [PROFICIENT RX LP]	1
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [PROFICIENT RX LP]	1
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [PROFICIENT RX LP]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET, FILM COATED [PROFICIENT RX LP]	1

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
I9W7N6B1KJ	FLUOXETINE HYDROCHLORIDE	56296-78-7	FLUOXETINE HYDROCHLORIDE
01K63SUP8D	FLUOXETINE	54910-89-3	Fluoxetine

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
0093-7188-01	00093718801	100 TABLET, FILM COATED in 1 BOTTLE (0093-7188-01)	2019-11-12	0000-00-00	No	No	Current
0093-7188-10	00093718810	1000 TABLET, FILM COATED in 1 BOTTLE (0093-7188-10)	2002-01-30	0000-00-00	No	No	Current
0093-7188-56	00093718856	30 TABLET, FILM COATED in 1 BOTTLE (0093-7188-56)	2002-01-30	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Fluoxetine	Proficient Rx LP	2022-10-01	HUMAN PRESCRIPTION DRUG LABEL	4
Fluoxetine	Teva Pharmaceuticals USA, Inc.	2022-02-28	HUMAN PRESCRIPTION DRUG LABEL	27