ZOFRAN

Product NDC: 0173-0447
11-digit product format: 001730447
Labeler code: 0173
Product ID: 0173-0447_611b5ddf-6ba0-4811-b040-29004102f56c
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: ondansetron hydrochloride
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: GlaxoSmithKline LLC
Application: NDA020103
Marketing category: NDA
Marketing start: 1993-02-11
Marketing end: 2020-02-29
Substance: ONDANSETRON HYDROCHLORIDE
Active strength: 8 mg/1
Pharmacologic classes: Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	0173-0447		D	Discontinued by firm		2026-08-03
excluded package	package	0173-0447	0173-0447-00	D	Discontinued by firm		2026-08-03

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 · 24 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	0173-0447-00	`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	0173-0447-00	`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	0173-0447-00	`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	0173-0447-00	`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	0173-0447-00	`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	0173-0447-00	`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	0173-0447-00	`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	0173-0447-00	`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	0173-0447-00	`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	0173-0447-00	`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	0173-0447-00	`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	0173-0447-00	`557ba5c1ecfa…`	`9c80585c8c6e…`

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

Orange Book products#

Current product rows page 1 of 1 · 3 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	RLD / RS	Approval date
N020103-001	ZOFRAN	ONDANSETRON HYDROCHLORIDE	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31
N020103-002	ZOFRAN	ONDANSETRON HYDROCHLORIDE	EQ 8MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31
N020103-003	ZOFRAN	ONDANSETRON HYDROCHLORIDE	EQ 24MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-08-27

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 4 · 123 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	N020103-001	ZOFRAN	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N020103-002	ZOFRAN	EQ 8MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N020103-003	ZOFRAN	EQ 24MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-08-27	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020103-001	ZOFRAN	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020103-002	ZOFRAN	EQ 8MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020103-003	ZOFRAN	EQ 24MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-08-27	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	N020103-001	ZOFRAN	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N020103-002	ZOFRAN	EQ 8MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N020103-003	ZOFRAN	EQ 24MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-08-27	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020103-001	ZOFRAN	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020103-002	ZOFRAN	EQ 8MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020103-003	ZOFRAN	EQ 24MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-08-27	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020103-001	ZOFRAN	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020103-002	ZOFRAN	EQ 8MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020103-003	ZOFRAN	EQ 24MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-08-27	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020103-001	ZOFRAN	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020103-002	ZOFRAN	EQ 8MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020103-003	ZOFRAN	EQ 24MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-08-27	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N020103-001	ZOFRAN	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N020103-002	ZOFRAN	EQ 8MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N020103-003	ZOFRAN	EQ 24MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-08-27	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N020103-001	ZOFRAN	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N020103-002	ZOFRAN	EQ 8MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N020103-003	ZOFRAN	EQ 24MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-08-27	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	N020103-001	ZOFRAN	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	N020103-002	ZOFRAN	EQ 8MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	N020103-003	ZOFRAN	EQ 24MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-08-27	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	N020103-001	ZOFRAN	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	N020103-002	ZOFRAN	EQ 8MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	N020103-003	ZOFRAN	EQ 24MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-08-27	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	N020103-001	ZOFRAN	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	N020103-002	ZOFRAN	EQ 8MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	N020103-003	ZOFRAN	EQ 24MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-08-27	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	N020103-001	ZOFRAN	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`301d65b070ca…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	N020103-002	ZOFRAN	EQ 8MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`301d65b070ca…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	N020103-003	ZOFRAN	EQ 24MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-08-27	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N020103-001	ZOFRAN	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N020103-002	ZOFRAN	EQ 8MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N020103-003	ZOFRAN	EQ 24MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-08-27	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	N020103-001	ZOFRAN	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1992-12-31	`8072bd15b7f6…`

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2019-12-13 00:20 UTC	2019-12	N020103-001	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N020103-002	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N020103-003	AB	1	`74a2ff9319b5…`
2022-03-09 01:35 UTC	2022-03	N020103-001	AB	1	`bb7c543d1eb4…`
2022-03-09 01:35 UTC	2022-03	N020103-002	AB	1	`bb7c543d1eb4…`
2022-03-09 01:35 UTC	2022-03	N020103-003	AB	1	`bb7c543d1eb4…`
2021-12-28 21:50 UTC	2021-12	N020103-001	AB	1	`782e0a99824c…`
2021-12-28 21:50 UTC	2021-12	N020103-002	AB	1	`782e0a99824c…`
2021-12-28 21:50 UTC	2021-12	N020103-003	AB	1	`782e0a99824c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N020103-001	AB	1	`87673890dc5c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N020103-002	AB	1	`87673890dc5c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N020103-003	AB	1	`87673890dc5c…`
2021-03-12 10:30 UTC	2021-03	N020103-001	AB	1	`5aa47cf7b7d7…`
2021-03-12 10:30 UTC	2021-03	N020103-002	AB	1	`5aa47cf7b7d7…`
2021-03-12 10:30 UTC	2021-03	N020103-003	AB	1	`5aa47cf7b7d7…`
2020-12-22 03:56 UTC	2020-12	N020103-001	AB	1	`8869cabd3fbd…`
2020-12-22 03:56 UTC	2020-12	N020103-002	AB	1	`8869cabd3fbd…`
2020-12-22 03:56 UTC	2020-12	N020103-003	AB	1	`8869cabd3fbd…`
2020-11-12 02:37 UTC	2020-11	N020103-001	AB	1	`c0c555d07b60…`
2020-11-12 02:37 UTC	2020-11	N020103-002	AB	1	`c0c555d07b60…`
2020-11-12 02:37 UTC	2020-11	N020103-003	AB	1	`c0c555d07b60…`
2019-12-14 00:12 UTC	2019-12	N020103-001	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	N020103-002	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	N020103-003	AB	1	`3f01610625f2…`
2019-09-15 20:21 UTC	2019-09	N020103-001	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	N020103-002	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	N020103-003	AB	1	`b00525d2431f…`
2019-07-19 19:46 UTC	2019-07	N020103-001	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	N020103-002	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	N020103-003	AB	1	`ea99ee380514…`

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0173-0447-00	EA - Each	0173-0447	16980d21-c065-4b78-b4b6-5331fcb21911	1	2012-07-24
0173-0447-02	EA - Each	0173-0447	5cd465d7-7cf2-45fb-8262-c224224f40eb	1	2012-07-24
0173-0447-04	EA - Each	0173-0447	91e271b5-d9b5-489b-b81a-ab171ea11386	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ONDANSETRON	ACTIVE INGREDIENT	4AF302ESOS	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
ONDANSETRON HYDROCHLORIDE	ACTIVE INGREDIENT	NMH84OZK2B	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
ONDANSETRON	ACTIVE MOIETY	4AF302ESOS	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
ANHYDROUS CITRIC ACID	INACTIVE INGREDIENT	XF417D3PSL	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
ASPARTAME	INACTIVE INGREDIENT	Z0H242BBR1	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
GELATIN	INACTIVE INGREDIENT	2G86QN327L	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
LACTOSE	INACTIVE INGREDIENT	J2B2A4N98G	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
MANNITOL	INACTIVE INGREDIENT	3OWL53L36A	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
METHYLPARABEN SODIUM	INACTIVE INGREDIENT	CR6K9C2NHK	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
PROPYLPARABEN SODIUM	INACTIVE INGREDIENT	625NNB0G9N	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
SODIUM BENZOATE	INACTIVE INGREDIENT	OJ245FE5EU	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
SODIUM CITRATE	INACTIVE INGREDIENT	1Q73Q2JULR	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
SORBITOL	INACTIVE INGREDIENT	506T60A25R	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
TRIACETIN	INACTIVE INGREDIENT	XHX3C3X673	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15
WATER	INACTIVE INGREDIENT	059QF0KO0R	ZOFRAN (ONDANSETRON HYDROCHLORIDE) SOLUTION ZOFRAN ODT (ONDANSETRON HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING ZOFRAN (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	15