dicloxacillin sodium
Generic: dicloxacillin sodium
Labeler: aurobindo pharma limitedDrug Facts
Product Profile
Brand Name
dicloxacillin sodium
Generic Name
dicloxacillin sodium
Labeler
aurobindo pharma limited
Dosage Form
CAPSULE
Routes
Active Ingredients
dicloxacillin sodium 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
59651-565
Product ID
59651-565_faee6e2d-1b9c-4121-bc22-41313539b366
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216845
Listing Expiration
2026-12-31
Marketing Start
2022-09-23
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59651565
Hyphenated Format
59651-565
Supplemental Identifiers
RxCUI
UNII
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
dicloxacillin sodium (source: ndc)
Generic Name
dicloxacillin sodium (source: ndc)
Application Number
ANDA216845 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (59651-565-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "faee6e2d-1b9c-4121-bc22-41313539b366", "openfda": {"unii": ["4HZT2V9KX0"], "rxcui": ["197595", "197596"], "spl_set_id": ["9074b5a6-850c-4144-9097-bb21073ee54d"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (59651-565-01)", "package_ndc": "59651-565-01", "marketing_start_date": "20220923"}], "brand_name": "DICLOXACILLIN SODIUM", "product_id": "59651-565_faee6e2d-1b9c-4121-bc22-41313539b366", "dosage_form": "CAPSULE", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "59651-565", "generic_name": "DICLOXACILLIN SODIUM", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DICLOXACILLIN SODIUM", "active_ingredients": [{"name": "DICLOXACILLIN SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA216845", "marketing_category": "ANDA", "marketing_start_date": "20220923", "listing_expiration_date": "20261231"}