amoxicillin
Generic: amoxicillin
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
amoxicillin
Generic Name
amoxicillin
Labeler
preferred pharmaceuticals inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
amoxicillin 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-8240
Product ID
68788-8240_8e79c23e-382b-4640-b0df-0e1cf42b6717
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065271
Listing Expiration
2027-12-31
Marketing Start
2022-08-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888240
Hyphenated Format
68788-8240
Supplemental Identifiers
RxCUI
UNII
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
ANDA065271 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 21 CAPSULE in 1 BOTTLE (68788-8240-2)
- 30 CAPSULE in 1 BOTTLE (68788-8240-3)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8e79c23e-382b-4640-b0df-0e1cf42b6717", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308182"], "spl_set_id": ["d6a33b28-f520-4a4c-b553-0ebd00558345"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 CAPSULE in 1 BOTTLE (68788-8240-2)", "package_ndc": "68788-8240-2", "marketing_start_date": "20220809"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68788-8240-3)", "package_ndc": "68788-8240-3", "marketing_start_date": "20220809"}], "brand_name": "Amoxicillin", "product_id": "68788-8240_8e79c23e-382b-4640-b0df-0e1cf42b6717", "dosage_form": "CAPSULE", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "68788-8240", "generic_name": "Amoxicillin", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "250 mg/1"}], "application_number": "ANDA065271", "marketing_category": "ANDA", "marketing_start_date": "20220809", "listing_expiration_date": "20271231"}