rifampin

Generic: rifampin

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

Drug Facts

Product Profile

Brand Name rifampin
Generic Name rifampin
Labeler hikma pharmaceuticals usa inc.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

rifampin 600 mg/1

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9230
Product ID 0143-9230_1a816eb9-6de4-4751-831b-d183254f36af
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205039
Listing Expiration 2026-12-31
Marketing Start 2016-03-03

Pharmacologic Class

Established (EPC)
rifamycin antibacterial [epc]
Chemical Structure
rifamycins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01439230
Hyphenated Format 0143-9230

Supplemental Identifiers

RxCUI
312821
UNII
VJT6J7R4TR
NUI
N0000175500 M0019113

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 rifampin (source: ndc)
Generic Name rifampin (source: ndc)
Application Number ANDA205039 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0143-9230-01)
source: ndc

Packages (1)

Ingredients (1)

rifampin (600 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "1a816eb9-6de4-4751-831b-d183254f36af", "openfda": {"nui": ["N0000175500", "M0019113"], "unii": ["VJT6J7R4TR"], "rxcui": ["312821"], "spl_set_id": ["cb59a48c-f66b-4ea0-809c-de0e4be2f8c2"], "pharm_class_cs": ["Rifamycins [CS]"], "pharm_class_epc": ["Rifamycin Antibacterial [EPC]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0143-9230-01)", "package_ndc": "0143-9230-01", "marketing_start_date": "20160303"}], "brand_name": "Rifampin", "product_id": "0143-9230_1a816eb9-6de4-4751-831b-d183254f36af", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Rifamycin Antibacterial [EPC]", "Rifamycins [CS]"], "product_ndc": "0143-9230", "generic_name": "Rifampin", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rifampin", "active_ingredients": [{"name": "RIFAMPIN", "strength": "600 mg/1"}], "application_number": "ANDA205039", "marketing_category": "ANDA", "marketing_start_date": "20160303", "listing_expiration_date": "20261231"}