quinine sulfate

Generic: quinine sulfate

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

Drug Facts

Product Profile

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

quinine sulfate 324 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-3002
Product ID 0093-3002_29ebf3c2-8351-43c3-82ac-3b118fb7faf6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091661
Listing Expiration 2026-12-31
Marketing Start 2012-09-28

Pharmacologic Class

Classes
antimalarial [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00933002
Hyphenated Format 0093-3002

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 ANDA091661 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 324 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (0093-3002-56)
source: ndc

Packages (1)

Ingredients (1)

quinine sulfate (324 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "29ebf3c2-8351-43c3-82ac-3b118fb7faf6", "openfda": {"unii": ["KF7Z0E0Q2B"], "rxcui": ["997010"], "spl_set_id": ["e782283e-2608-4fd6-a8b2-6c30b9d5d3b0"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (0093-3002-56)", "package_ndc": "0093-3002-56", "marketing_start_date": "20120928"}], "brand_name": "Quinine Sulfate", "product_id": "0093-3002_29ebf3c2-8351-43c3-82ac-3b118fb7faf6", "dosage_form": "CAPSULE", "pharm_class": ["Antimalarial [EPC]"], "product_ndc": "0093-3002", "generic_name": "Quinine Sulfate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quinine Sulfate", "active_ingredients": [{"name": "QUININE SULFATE", "strength": "324 mg/1"}], "application_number": "ANDA091661", "marketing_category": "ANDA", "marketing_start_date": "20120928", "listing_expiration_date": "20261231"}