amoxicillin

Generic: amoxicillin

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amoxicillin
Generic Name amoxicillin
Labeler american health packaging
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

amoxicillin 500 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-798
Product ID 60687-798_3a9c47e7-eec8-42b3-e063-6294a90afa26
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065256
Listing Expiration 2026-12-31
Marketing Start 2025-03-25

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687798
Hyphenated Format 60687-798

Supplemental Identifiers

RxCUI
308192 308194
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 ANDA065256 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (60687-798-25) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-798-95)
source: ndc

Packages (1)

Ingredients (1)

amoxicillin (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a9c47e7-eec8-42b3-e063-6294a90afa26", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308192", "308194"], "spl_set_id": ["d339ea0f-8797-460f-a3b7-b8455c250366"], "manufacturer_name": ["American Health Packaging"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (60687-798-25)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-798-95)", "package_ndc": "60687-798-25", "marketing_start_date": "20250325"}], "brand_name": "Amoxicillin", "product_id": "60687-798_3a9c47e7-eec8-42b3-e063-6294a90afa26", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "60687-798", "generic_name": "Amoxicillin", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "500 mg/1"}], "application_number": "ANDA065256", "marketing_category": "ANDA", "marketing_start_date": "20250325", "listing_expiration_date": "20261231"}