ondansetron hydrochloride

Generic: ondansetron hydrochloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ondansetron hydrochloride
Generic Name ondansetron hydrochloride
Labeler american health packaging
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ondansetron hydrochloride 8 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 68084-221
Product ID 68084-221_276fcece-7658-5e70-e063-6394a90a91ae
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078539
Listing Expiration 2026-12-31
Marketing Start 2023-09-21

Pharmacologic Class

Classes
serotonin 3 receptor antagonists [moa] serotonin-3 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68084221
Hyphenated Format 68084-221

Supplemental Identifiers

RxCUI
198052 312086
UNII
NMH84OZK2B

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ondansetron hydrochloride (source: ndc)
Generic Name ondansetron hydrochloride (source: ndc)
Application Number ANDA078539 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 8 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-221-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-221-11)
source: ndc

Packages (1)

68084-221-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-221-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-221-11)

Ingredients (1)

ondansetron hydrochloride (8 mg/1)

Linked Drug Pages (1)

Ondansetron Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "276fcece-7658-5e70-e063-6394a90a91ae", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["198052", "312086"], "spl_set_id": ["9f015e60-1aec-4ae7-b28f-42f6c8f50455"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-221-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-221-11)", "package_ndc": "68084-221-01", "marketing_start_date": "20230921"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "68084-221_276fcece-7658-5e70-e063-6394a90a91ae", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "68084-221", "generic_name": "Ondansetron Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron Hydrochloride", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "8 mg/1"}], "application_number": "ANDA078539", "marketing_category": "ANDA", "marketing_start_date": "20230921", "listing_expiration_date": "20261231"}