amoxicillin

Generic: amoxicillin

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

amoxicillin 250 mg/5mL

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-777
Product ID 62135-777_4690a5fd-79cc-e1fd-e063-6294a90a009c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA062059
Listing Expiration 2026-12-31
Marketing Start 1978-12-08

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135777
Hyphenated Format 62135-777

Supplemental Identifiers

RxCUI
239191 313797
UPC
0362135776381 0362135777388
UNII
804826J2HU

Packaging Origin

Original Packager
true

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 ANDA062059 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/5mL
source: ndc
Packaging
  • 150 mL in 1 BOTTLE (62135-777-38)
  • 100 mL in 1 BOTTLE (62135-777-42)
  • 80 mL in 1 BOTTLE (62135-777-68)
source: ndc

Packages (3)

Ingredients (1)

amoxicillin (250 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4690a5fd-79cc-e1fd-e063-6294a90a009c", "openfda": {"upc": ["0362135776381", "0362135777388"], "unii": ["804826J2HU"], "rxcui": ["239191", "313797"], "spl_set_id": ["9ce26893-c7a1-47e9-98f9-f5d998cac418"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "150 mL in 1 BOTTLE (62135-777-38)", "package_ndc": "62135-777-38", "marketing_start_date": "20231215"}, {"sample": false, "description": "100 mL in 1 BOTTLE (62135-777-42)", "package_ndc": "62135-777-42", "marketing_start_date": "20231215"}, {"sample": false, "description": "80 mL in 1 BOTTLE (62135-777-68)", "package_ndc": "62135-777-68", "marketing_start_date": "20231215"}], "brand_name": "AMOXICILLIN", "product_id": "62135-777_4690a5fd-79cc-e1fd-e063-6294a90a009c", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "62135-777", "generic_name": "Amoxicillin", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMOXICILLIN", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "250 mg/5mL"}], "application_number": "ANDA062059", "marketing_category": "ANDA", "marketing_start_date": "19781208", "listing_expiration_date": "20261231"}