amoxicillin

Generic: amoxicillin

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amoxicillin
Generic Name amoxicillin
Labeler hikma pharmaceuticals usa inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

amoxicillin 500 mg/1

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9939
Product ID 0143-9939_ede2b8f8-5f17-494b-8dd9-a3368f76aebf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065291
Listing Expiration 2027-12-31
Marketing Start 2007-03-01

Pharmacologic Class

Classes
penicillin-class antibacterial [epc] penicillins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01439939
Hyphenated Format 0143-9939

Supplemental Identifiers

UNII
804826J2HU

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 amoxicillin (source: ndc)
Generic Name amoxicillin (source: ndc)
Application Number ANDA065291 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 500 CAPSULE in 1 BOTTLE, PLASTIC (0143-9939-05)
source: ndc

Packages (1)

Ingredients (1)

amoxicillin (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ede2b8f8-5f17-494b-8dd9-a3368f76aebf", "openfda": {"unii": ["804826J2HU"], "spl_set_id": ["4fb7837e-964c-4d38-a3a5-b384b1bd6e08"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE, PLASTIC (0143-9939-05)", "package_ndc": "0143-9939-05", "marketing_start_date": "20070301"}], "brand_name": "Amoxicillin", "product_id": "0143-9939_ede2b8f8-5f17-494b-8dd9-a3368f76aebf", "dosage_form": "CAPSULE", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "0143-9939", "generic_name": "Amoxicillin", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "500 mg/1"}], "application_number": "ANDA065291", "marketing_category": "ANDA", "marketing_start_date": "20070301", "listing_expiration_date": "20271231"}