amoxicillin

Generic: amoxicillin

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

amoxicillin 400 mg/5mL

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 61919-401
Product ID 61919-401_0e877b33-af19-d857-e063-6394a90a08ea
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065334
Listing Expiration 2026-12-31
Marketing Start 2014-01-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 61919401
Hyphenated Format 61919-401

Supplemental Identifiers

RxCUI
308189 617296
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 ANDA065334 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/5mL
source: ndc
Packaging
  • 100 mL in 1 BOTTLE (61919-401-32)
source: ndc

Packages (1)

61919-401-32 100 mL in 1 BOTTLE (61919-401-32)

Ingredients (1)

amoxicillin (400 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": "0e877b33-af19-d857-e063-6394a90a08ea", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308189", "617296"], "spl_set_id": ["0173e9de-a995-4386-bb65-8fc2bbf347f9"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (61919-401-32)", "package_ndc": "61919-401-32", "marketing_start_date": "20200619"}], "brand_name": "AMOXICILLIN", "product_id": "61919-401_0e877b33-af19-d857-e063-6394a90a08ea", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "61919-401", "generic_name": "AMOXICILLIN", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMOXICILLIN", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "400 mg/5mL"}], "application_number": "ANDA065334", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}