paclitaxel
Generic: paclitaxel
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
paclitaxel
Generic Name
paclitaxel
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
paclitaxel 6 mg/mL
Manufacturer
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)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
61703342
Hyphenated Format
61703-342
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 6 mg/mL
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
Packages (3)
Ingredients (1)
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"}