quinine sulfate

Generic: quinine sulfate

Labeler: ingenus pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name quinine sulfate
Generic Name quinine sulfate
Labeler ingenus pharmaceuticals, llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

quinine sulfate 324 mg/1

Manufacturer
Ingenus Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 50742-238
Product ID 50742-238_0a0b38d3-828f-4828-8d8c-92933872aa4f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204372
Listing Expiration 2026-12-31
Marketing Start 2017-12-11

Pharmacologic Class

Classes
antimalarial [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50742238
Hyphenated Format 50742-238

Supplemental Identifiers

RxCUI
997010
UPC
0350742238309
UNII
KF7Z0E0Q2B

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 quinine sulfate (source: ndc)
Generic Name quinine sulfate (source: ndc)
Application Number ANDA204372 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 324 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (50742-238-30)
source: ndc

Packages (1)

50742-238-30 30 CAPSULE in 1 BOTTLE, PLASTIC (50742-238-30)

Ingredients (1)

quinine sulfate (324 mg/1)

Linked Drug Pages (1)

QUININE SULFATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0a0b38d3-828f-4828-8d8c-92933872aa4f", "openfda": {"upc": ["0350742238309"], "unii": ["KF7Z0E0Q2B"], "rxcui": ["997010"], "spl_set_id": ["b2f73c64-b92c-49bf-ad39-e32ac83e4d3d"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (50742-238-30)", "package_ndc": "50742-238-30", "marketing_start_date": "20171211"}], "brand_name": "QUININE SULFATE", "product_id": "50742-238_0a0b38d3-828f-4828-8d8c-92933872aa4f", "dosage_form": "CAPSULE", "pharm_class": ["Antimalarial [EPC]"], "product_ndc": "50742-238", "generic_name": "QUININE SULFATE", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "QUININE SULFATE", "active_ingredients": [{"name": "QUININE SULFATE", "strength": "324 mg/1"}], "application_number": "ANDA204372", "marketing_category": "ANDA", "marketing_start_date": "20171211", "listing_expiration_date": "20261231"}