paclitaxel

Generic: paclitaxel

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

Drug Facts

Product Profile

Brand Name paclitaxel
Generic Name paclitaxel
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

paclitaxel 6 mg/mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 61703-342
Product ID 61703-342_f4f04a49-a3f6-40cd-b261-aa889a0b7d0d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076131
Listing Expiration 2026-12-31
Marketing Start 2004-03-01

Pharmacologic Class

Established (EPC)
microtubule inhibitor [epc]
Physiologic Effect
microtubule inhibition [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 61703342
Hyphenated Format 61703-342

Supplemental Identifiers

RxCUI
312199
UNII
P88XT4IS4D
NUI
N0000175085 N0000175592

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 paclitaxel (source: ndc)
Generic Name paclitaxel (source: ndc)
Application Number ANDA076131 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 6 mg/mL
source: ndc
Packaging
  • 1 VIAL, MULTI-DOSE in 1 CARTON (61703-342-09) / 5 mL in 1 VIAL, MULTI-DOSE
  • 1 VIAL, MULTI-DOSE in 1 CARTON (61703-342-22) / 16.7 mL in 1 VIAL, MULTI-DOSE
  • 1 VIAL, MULTI-DOSE in 1 CARTON (61703-342-50) / 50 mL in 1 VIAL, MULTI-DOSE
source: ndc

Packages (3)

Ingredients (1)

paclitaxel (6 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f4f04a49-a3f6-40cd-b261-aa889a0b7d0d", "openfda": {"nui": ["N0000175085", "N0000175592"], "unii": ["P88XT4IS4D"], "rxcui": ["312199"], "spl_set_id": ["ea28753a-8631-460a-bfdc-b101eb8ac84a"], "pharm_class_pe": ["Microtubule Inhibition [PE]"], "pharm_class_epc": ["Microtubule Inhibitor [EPC]"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (61703-342-09)  / 5 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "61703-342-09", "marketing_start_date": "20040301"}, {"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (61703-342-22)  / 16.7 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "61703-342-22", "marketing_start_date": "20040301"}, {"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (61703-342-50)  / 50 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "61703-342-50", "marketing_start_date": "20040301"}], "brand_name": "Paclitaxel", "product_id": "61703-342_f4f04a49-a3f6-40cd-b261-aa889a0b7d0d", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "61703-342", "generic_name": "PACLITAXEL", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paclitaxel", "active_ingredients": [{"name": "PACLITAXEL", "strength": "6 mg/mL"}], "application_number": "ANDA076131", "marketing_category": "ANDA", "marketing_start_date": "20040301", "listing_expiration_date": "20261231"}