Home NDC 76420-916 Ondansetron Hydrochloride
Product NDC 76420-916
11-digit product format 764200916
Labeler code 76420
Product ID 76420-916_2cbe06c2-92c4-f72d-e063-6294a90aede8
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Ondansetron Hydrochloride
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Asclemed USA, Inc.
Application ANDA078539
Marketing category ANDA
Marketing start 2007-07-31
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 2027-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 44 .
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 TE codes RLD / RS Approval date A078539-001 ONDANSETRON HYDROCHLORIDE ONDANSETRON HYDROCHLORIDE EQ 4MG BASE TABLET / ORAL AB 2007-07-31 A078539-002 ONDANSETRON HYDROCHLORIDE ONDANSETRON HYDROCHLORIDE EQ 8MG BASE TABLET / ORAL AB 2007-07-31 A078539-003 ONDANSETRON HYDROCHLORIDE ONDANSETRON HYDROCHLORIDE EQ 24MG BASE TABLET / ORAL 2007-07-31
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 2 matching rows.
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 · 132 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-10-15 13:18:30 2026-09 A078539-001 ONDANSETRON HYDROCHLORIDE EQ 4MG BASE TABLET / ORAL AB 2007-07-31 c2088c7a36db…2026-10-15 13:18:30 2026-09 A078539-002 ONDANSETRON HYDROCHLORIDE EQ 8MG BASE TABLET / ORAL AB 2007-07-31 c2088c7a36db…2026-10-15 13:18:30 2026-09 A078539-003 ONDANSETRON HYDROCHLORIDE EQ 24MG BASE TABLET / ORAL 2007-07-31 c2088c7a36db…2026-09-14 22:38:34 2026-08 A078539-001 ONDANSETRON HYDROCHLORIDE EQ 4MG BASE TABLET / ORAL AB 2007-07-31 84e616aacf4f…2026-09-14 22:38:34 2026-08 A078539-002 ONDANSETRON HYDROCHLORIDE EQ 8MG BASE TABLET / ORAL AB 2007-07-31 84e616aacf4f…2026-09-14 22:38:34 2026-08 A078539-003 ONDANSETRON HYDROCHLORIDE EQ 24MG BASE TABLET / ORAL 2007-07-31 84e616aacf4f…2026-08-18 06:07:40 2026-07 A078539-001 ONDANSETRON HYDROCHLORIDE EQ 4MG BASE TABLET / ORAL AB 2007-07-31 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A078539-002 ONDANSETRON HYDROCHLORIDE EQ 8MG BASE TABLET / ORAL AB 2007-07-31 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A078539-003 ONDANSETRON HYDROCHLORIDE EQ 24MG BASE TABLET / ORAL 2007-07-31 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A078539-001 ONDANSETRON HYDROCHLORIDE EQ 4MG BASE TABLET / ORAL AB 2007-07-31 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A078539-002 ONDANSETRON HYDROCHLORIDE EQ 8MG BASE TABLET / ORAL AB 2007-07-31 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A078539-003 ONDANSETRON HYDROCHLORIDE EQ 24MG BASE TABLET / ORAL 2007-07-31 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A078539-001 ONDANSETRON HYDROCHLORIDE EQ 4MG BASE TABLET / ORAL AB 2007-07-31 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A078539-002 ONDANSETRON HYDROCHLORIDE EQ 8MG BASE TABLET / ORAL AB 2007-07-31 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A078539-003 ONDANSETRON HYDROCHLORIDE EQ 24MG BASE TABLET / ORAL 2007-07-31 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A078539-001 ONDANSETRON HYDROCHLORIDE EQ 4MG BASE TABLET / ORAL AB 2007-07-31 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A078539-002 ONDANSETRON HYDROCHLORIDE EQ 8MG BASE TABLET / ORAL AB 2007-07-31 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A078539-003 ONDANSETRON HYDROCHLORIDE EQ 24MG BASE TABLET / ORAL 2007-07-31 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A078539-001 ONDANSETRON HYDROCHLORIDE EQ 4MG BASE TABLET / ORAL AB 2007-07-31 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A078539-002 ONDANSETRON HYDROCHLORIDE EQ 8MG BASE TABLET / ORAL AB 2007-07-31 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A078539-003 ONDANSETRON HYDROCHLORIDE EQ 24MG BASE TABLET / ORAL 2007-07-31 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A078539-001 ONDANSETRON HYDROCHLORIDE EQ 4MG BASE TABLET / ORAL AB 2007-07-31 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A078539-002 ONDANSETRON HYDROCHLORIDE EQ 8MG BASE TABLET / ORAL AB 2007-07-31 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A078539-003 ONDANSETRON HYDROCHLORIDE EQ 24MG BASE TABLET / ORAL 2007-07-31 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A078539-001 ONDANSETRON HYDROCHLORIDE EQ 4MG BASE TABLET / ORAL AB 2007-07-31 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A078539-002 ONDANSETRON HYDROCHLORIDE EQ 8MG BASE TABLET / ORAL AB 2007-07-31 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A078539-003 ONDANSETRON HYDROCHLORIDE EQ 24MG BASE TABLET / ORAL 2007-07-31 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A078539-001 ONDANSETRON HYDROCHLORIDE EQ 4MG BASE TABLET / ORAL AB 2007-07-31 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A078539-002 ONDANSETRON HYDROCHLORIDE EQ 8MG BASE TABLET / ORAL AB 2007-07-31 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A078539-003 ONDANSETRON HYDROCHLORIDE EQ 24MG BASE TABLET / ORAL 2007-07-31 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A078539-001 ONDANSETRON HYDROCHLORIDE EQ 4MG BASE TABLET / ORAL AB 2007-07-31 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A078539-002 ONDANSETRON HYDROCHLORIDE EQ 8MG BASE TABLET / ORAL AB 2007-07-31 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A078539-003 ONDANSETRON HYDROCHLORIDE EQ 24MG BASE TABLET / ORAL 2007-07-31 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A078539-001 ONDANSETRON HYDROCHLORIDE EQ 4MG BASE TABLET / ORAL AB 2007-07-31 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A078539-002 ONDANSETRON HYDROCHLORIDE EQ 8MG BASE TABLET / ORAL AB 2007-07-31 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A078539-003 ONDANSETRON HYDROCHLORIDE EQ 24MG BASE TABLET / ORAL 2007-07-31 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 A078539-001 ONDANSETRON HYDROCHLORIDE EQ 4MG BASE TABLET / ORAL AB 2007-07-31 d06236e962d9…2024-10-29 15:01 UTC 2024-10 A078539-002 ONDANSETRON HYDROCHLORIDE EQ 8MG BASE TABLET / ORAL AB 2007-07-31 d06236e962d9…2024-10-29 15:01 UTC 2024-10 A078539-003 ONDANSETRON HYDROCHLORIDE EQ 24MG BASE TABLET / ORAL 2007-07-31 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A078539-001 ONDANSETRON HYDROCHLORIDE EQ 4MG BASE TABLET / ORAL AB 2007-07-31 79d66fd596c7…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 3 · 98 observed states.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Ondansetron Hydrochloride
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ONDANSETRON HYDROCHLORIDE 8 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination NMH84OZK2B Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198052 Internal RxNorm lookup 312084 Internal RxNorm lookup 312086 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 76420-916-00 Ondansetron Hydrochloride 1000 in 1 BOTTLE TABLET, FILM COATED 1000 1 76420-916-03 Ondansetron Hydrochloride 3 in 1 BOTTLE TABLET, FILM COATED 3 1 76420-916-05 Ondansetron Hydrochloride 500 in 1 BOTTLE TABLET, FILM COATED 500 1 76420-916-10 Ondansetron Hydrochloride 10 in 1 BOTTLE TABLET, FILM COATED 10 1 76420-916-11 Ondansetron Hydrochloride 10 in 1 BLISTER PACK TABLET, FILM COATED 10 1 76420-916-11 Ondansetron Hydrochloride 10 in 1 CARTON TABLET, FILM COATED 10 1 76420-916-30 Ondansetron Hydrochloride 30 in 1 BOTTLE TABLET, FILM COATED 30 1 76420-916-33 Ondansetron Hydrochloride 3 in 1 BLISTER PACK TABLET, FILM COATED 3 1 76420-916-33 Ondansetron Hydrochloride 1 in 1 CARTON TABLET, FILM COATED 1 1 76420-916-60 Ondansetron Hydrochloride 60 in 1 BOTTLE TABLET, FILM COATED 60 1 76420-916-90 Ondansetron Hydrochloride 90 in 1 BOTTLE TABLET, FILM COATED 90 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76420-916 ONDANSETRON HYDROCHLORIDE TABLET, FILM COATED ONDANSETRON HYDROCHLORIDE (ONDANSETRON HYDROCHLORIDE) TABLET, FILM COATED [ASCLEMED USA, INC.] 1 Current NDC, 11 package rows 20250130_65b0b2e2-37fd-4d08-9674-954d62bb531a.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 4 of 4 · 63 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 76420-916-00 76420091600 1000 TABLET, FILM COATED in 1 BOTTLE (76420-916-00) 2025-01-28 No No Current 76420-916-03 76420091603 3 TABLET, FILM COATED in 1 BOTTLE (76420-916-03) 2025-01-28 No No Current 76420-916-05 76420091605 500 TABLET, FILM COATED in 1 BOTTLE (76420-916-05) 2025-01-28 No No Current 76420-916-10 76420091610 10 TABLET, FILM COATED in 1 BOTTLE (76420-916-10) 2025-01-28 No No Current 76420-916-11 76420091611 10 BLISTER PACK in 1 CARTON (76420-916-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK 10 blister pack 2025-01-28 No No Current 76420-916-30 76420091630 30 TABLET, FILM COATED in 1 BOTTLE (76420-916-30) 2025-01-28 No No Current 76420-916-33 76420091633 1 BLISTER PACK in 1 CARTON (76420-916-33) / 3 TABLET, FILM COATED in 1 BLISTER PACK 1 blister pack 2025-01-28 No No Current 76420-916-60 76420091660 60 TABLET, FILM COATED in 1 BOTTLE (76420-916-60) 2025-01-28 No No Current 76420-916-90 76420091690 90 TABLET, FILM COATED in 1 BOTTLE (76420-916-90) 2025-01-28 No No Current