dicloxacillin sodium
Generic: dicloxacillin sodium
Labeler: teva pharmaceuticals usa, inc.Drug Facts
Product Profile
Brand Name
dicloxacillin sodium
Generic Name
dicloxacillin sodium
Labeler
teva pharmaceuticals usa, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
dicloxacillin sodium 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0093-3125
Product ID
0093-3125_1976304d-7c32-40f7-9724-0d1903dad50e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062286
Listing Expiration
2026-12-31
Marketing Start
1990-09-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00933125
Hyphenated Format
0093-3125
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
ANDA062286 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (0093-3125-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1976304d-7c32-40f7-9724-0d1903dad50e", "openfda": {"unii": ["4HZT2V9KX0"], "rxcui": ["197595", "197596"], "spl_set_id": ["8478f242-c715-4984-ac1d-dc79dc28665e"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0093-3125-01)", "package_ndc": "0093-3125-01", "marketing_start_date": "19900930"}], "brand_name": "Dicloxacillin Sodium", "product_id": "0093-3125_1976304d-7c32-40f7-9724-0d1903dad50e", "dosage_form": "CAPSULE", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "0093-3125", "generic_name": "Dicloxacillin Sodium", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicloxacillin Sodium", "active_ingredients": [{"name": "DICLOXACILLIN SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA062286", "marketing_category": "ANDA", "marketing_start_date": "19900930", "listing_expiration_date": "20261231"}