atovaquone

Generic: atovaquone

Labeler: northstar rxllc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atovaquone
Generic Name atovaquone
Labeler northstar rxllc
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

atovaquone 750 mg/5mL

Manufacturer
NorthStar RxLLC

Identifiers & Regulatory

Product NDC 72603-248
Product ID 72603-248_15e36ffa-2f19-ac0a-e063-6394a90afe22
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210692
Listing Expiration 2026-12-31
Marketing Start 2024-05-01

Pharmacologic Class

Established (EPC)
antimalarial [epc] antiprotozoal [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72603248
Hyphenated Format 72603-248

Supplemental Identifiers

RxCUI
308429
UPC
0372603248012
UNII
Y883P1Z2LT
NUI
N0000175482 N0000175485

Packaging Origin

Original Packager
true

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 atovaquone (source: ndc)
Generic Name atovaquone (source: ndc)
Application Number ANDA210692 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/5mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (72603-248-01) / 210 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

atovaquone (750 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "15e36ffa-2f19-ac0a-e063-6394a90afe22", "openfda": {"nui": ["N0000175482", "N0000175485"], "upc": ["0372603248012"], "unii": ["Y883P1Z2LT"], "rxcui": ["308429"], "spl_set_id": ["fc7bdd97-f780-4eed-80e0-72e70267b21a"], "pharm_class_epc": ["Antimalarial [EPC]", "Antiprotozoal [EPC]"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (72603-248-01)  / 210 mL in 1 BOTTLE", "package_ndc": "72603-248-01", "marketing_start_date": "20240501"}], "brand_name": "Atovaquone", "product_id": "72603-248_15e36ffa-2f19-ac0a-e063-6394a90afe22", "dosage_form": "SUSPENSION", "pharm_class": ["Antimalarial [EPC]", "Antiprotozoal [EPC]"], "product_ndc": "72603-248", "generic_name": "Atovaquone", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atovaquone", "active_ingredients": [{"name": "ATOVAQUONE", "strength": "750 mg/5mL"}], "application_number": "ANDA210692", "marketing_category": "ANDA", "marketing_start_date": "20240501", "listing_expiration_date": "20261231"}