amoxicillin

Generic: amoxicillin

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amoxicillin
Generic Name amoxicillin
Labeler pd-rx pharmaceuticals, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

amoxicillin 500 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-225
Product ID 72789-225_40ad11b9-8247-8d3f-e063-6294a90a26eb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065291
Listing Expiration 2026-12-31
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 72789225
Hyphenated Format 72789-225

Supplemental Identifiers

RxCUI
308191
UPC
0372789225821
UNII
804826J2HU

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 (72789-225-82)
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": "40ad11b9-8247-8d3f-e063-6294a90a26eb", "openfda": {"upc": ["0372789225821"], "unii": ["804826J2HU"], "rxcui": ["308191"], "spl_set_id": ["96057ce7-9516-4239-9974-5e9691b44c9b"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE, PLASTIC (72789-225-82)", "package_ndc": "72789-225-82", "marketing_start_date": "20220210"}], "brand_name": "Amoxicillin", "product_id": "72789-225_40ad11b9-8247-8d3f-e063-6294a90a26eb", "dosage_form": "CAPSULE", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "72789-225", "generic_name": "Amoxicillin", "labeler_name": "PD-Rx Pharmaceuticals, 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": "20261231"}