capecitabine

Generic: capecitabine

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name capecitabine
Generic Name capecitabine
Labeler american health packaging
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

capecitabine 500 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-149
Product ID 60687-149_3ccf2d80-f89f-9695-e063-6294a90abf27
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091649
Listing Expiration 2026-12-31
Marketing Start 2016-03-07

Pharmacologic Class

Established (EPC)
nucleoside metabolic inhibitor [epc]
Mechanism of Action
nucleic acid synthesis inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687149
Hyphenated Format 60687-149

Supplemental Identifiers

RxCUI
200328
UNII
6804DJ8Z9U
NUI
N0000000233 N0000175595

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 capecitabine (source: ndc)
Generic Name capecitabine (source: ndc)
Application Number ANDA091649 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 20 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-149-94) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-149-11)
source: ndc

Packages (1)

60687-149-94 20 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-149-94) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-149-11)

Ingredients (1)

capecitabine (500 mg/1)

Linked Drug Pages (1)

Capecitabine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ccf2d80-f89f-9695-e063-6294a90abf27", "openfda": {"nui": ["N0000000233", "N0000175595"], "unii": ["6804DJ8Z9U"], "rxcui": ["200328"], "spl_set_id": ["2777b481-7d7f-461a-b5e0-c09ce2990c34"], "pharm_class_epc": ["Nucleoside Metabolic Inhibitor [EPC]"], "pharm_class_moa": ["Nucleic Acid Synthesis Inhibitors [MoA]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-149-94)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-149-11)", "package_ndc": "60687-149-94", "marketing_start_date": "20160307"}], "brand_name": "Capecitabine", "product_id": "60687-149_3ccf2d80-f89f-9695-e063-6294a90abf27", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Nucleic Acid Synthesis Inhibitors [MoA]", "Nucleoside Metabolic Inhibitor [EPC]"], "product_ndc": "60687-149", "generic_name": "Capecitabine", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Capecitabine", "active_ingredients": [{"name": "CAPECITABINE", "strength": "500 mg/1"}], "application_number": "ANDA091649", "marketing_category": "ANDA", "marketing_start_date": "20160307", "listing_expiration_date": "20261231"}