quinine sulfate

Generic: quinine sulfate

Labeler: lupin pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name quinine sulfate
Generic Name quinine sulfate
Labeler lupin pharmaceuticals, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

quinine sulfate 324 mg/1

Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-560
Product ID 68180-560_8cd4d427-50ac-4f9c-a029-e7c2d063679a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203112
Listing Expiration 2026-12-31
Marketing Start 2015-08-04

Pharmacologic Class

Classes
antimalarial [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68180560
Hyphenated Format 68180-560

Supplemental Identifiers

RxCUI
997010
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 ANDA203112 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 324 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (68180-560-06)
source: ndc

Packages (1)

68180-560-06 30 CAPSULE in 1 BOTTLE (68180-560-06)

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": "8cd4d427-50ac-4f9c-a029-e7c2d063679a", "openfda": {"unii": ["KF7Z0E0Q2B"], "rxcui": ["997010"], "spl_set_id": ["1f32f05c-a215-40be-b951-e41a7b54a8a0"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68180-560-06)", "package_ndc": "68180-560-06", "marketing_start_date": "20150804"}], "brand_name": "QUININE SULFATE", "product_id": "68180-560_8cd4d427-50ac-4f9c-a029-e7c2d063679a", "dosage_form": "CAPSULE", "pharm_class": ["Antimalarial [EPC]"], "product_ndc": "68180-560", "generic_name": "QUININE SULFATE", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "QUININE SULFATE", "active_ingredients": [{"name": "QUININE SULFATE", "strength": "324 mg/1"}], "application_number": "ANDA203112", "marketing_category": "ANDA", "marketing_start_date": "20150804", "listing_expiration_date": "20261231"}