amoxil

Generic: amoxicillin oral susp

Labeler: directrx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amoxil
Generic Name amoxicillin oral susp
Labeler directrx
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

amoxicillin 400 mg/5mL

Manufacturer
DirectRx

Identifiers & Regulatory

Product NDC 72189-385
Product ID 72189-385_2c4cbe6c-c27d-15fe-e063-6294a90ac409
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065325
Listing Expiration 2026-12-31
Marketing Start 2022-10-21

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189385
Hyphenated Format 72189-385

Supplemental Identifiers

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 amoxil (source: ndc)
Generic Name amoxicillin oral susp (source: ndc)
Application Number ANDA065325 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/5mL
source: ndc
Packaging
  • 100 mL in 1 BOTTLE (72189-385-32)
source: ndc

Packages (1)

72189-385-32 100 mL in 1 BOTTLE (72189-385-32)

Ingredients (1)

amoxicillin (400 mg/5mL)

Linked Drug Pages (1)

Amoxil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4cbe6c-c27d-15fe-e063-6294a90ac409", "openfda": {"unii": ["804826J2HU"], "spl_set_id": ["ec7dd735-dc92-3d29-e053-2a95a90af549"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (72189-385-32)", "package_ndc": "72189-385-32", "marketing_start_date": "20221021"}], "brand_name": "Amoxil", "product_id": "72189-385_2c4cbe6c-c27d-15fe-e063-6294a90ac409", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "72189-385", "generic_name": "Amoxicillin Oral Susp", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxil", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "400 mg/5mL"}], "application_number": "ANDA065325", "marketing_category": "ANDA", "marketing_start_date": "20221021", "listing_expiration_date": "20261231"}