amoxicillin

Generic: amoxicillin

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amoxicillin
Generic Name amoxicillin
Labeler proficient rx lp
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

amoxicillin 250 mg/5mL

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-134
Product ID 82804-134_c8e5ad7d-09b7-41d9-8cb0-467b3e8df74f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204030
Listing Expiration 2026-12-31
Marketing Start 2014-09-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804134
Hyphenated Format 82804-134

Supplemental Identifiers

RxCUI
239191
UPC
0382804134151
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 ANDA204030 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/5mL
source: ndc
Packaging
  • 150 mL in 1 BOTTLE (82804-134-15)
source: ndc

Packages (1)

82804-134-15 150 mL in 1 BOTTLE (82804-134-15)

Ingredients (1)

amoxicillin (250 mg/5mL)

Linked Drug Pages (1)

Amoxicillin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c8e5ad7d-09b7-41d9-8cb0-467b3e8df74f", "openfda": {"upc": ["0382804134151"], "unii": ["804826J2HU"], "rxcui": ["239191"], "spl_set_id": ["c8e5ad7d-09b7-41d9-8cb0-467b3e8df74f"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "150 mL in 1 BOTTLE (82804-134-15)", "package_ndc": "82804-134-15", "marketing_start_date": "20240815"}], "brand_name": "Amoxicillin", "product_id": "82804-134_c8e5ad7d-09b7-41d9-8cb0-467b3e8df74f", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "82804-134", "generic_name": "Amoxicillin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "250 mg/5mL"}], "application_number": "ANDA204030", "marketing_category": "ANDA", "marketing_start_date": "20140915", "listing_expiration_date": "20261231"}