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 TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

amoxicillin 250 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-341
Product ID 43063-341_3a24c129-074d-c363-e063-6394a90a3a3a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA064013
Listing Expiration 2026-12-31
Marketing Start 1993-01-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43063341
Hyphenated Format 43063-341

Supplemental Identifiers

RxCUI
598025
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 ANDA064013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 4 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (43063-341-04)
source: ndc

Packages (1)

Ingredients (1)

amoxicillin (250 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a24c129-074d-c363-e063-6394a90a3a3a", "openfda": {"unii": ["804826J2HU"], "rxcui": ["598025"], "spl_set_id": ["09660a95-a7b3-4d1f-832c-a4fa7a5b7ddd"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (43063-341-04)", "package_ndc": "43063-341-04", "marketing_start_date": "20111126"}], "brand_name": "Amoxicillin", "product_id": "43063-341_3a24c129-074d-c363-e063-6394a90a3a3a", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "43063-341", "generic_name": "Amoxicillin", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "250 mg/1"}], "application_number": "ANDA064013", "marketing_category": "ANDA", "marketing_start_date": "19930101", "listing_expiration_date": "20261231"}