amoxicillin
Generic: amoxicillin
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
amoxicillin
Generic Name
amoxicillin
Labeler
bryant ranch prepack
Dosage Form
CAPSULE
Routes
Active Ingredients
amoxicillin 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63629-5739
Product ID
63629-5739_7f38a7aa-45bb-4d8c-9595-89fba63cdc96
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065271
Listing Expiration
2026-12-31
Marketing Start
2005-11-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636295739
Hyphenated Format
63629-5739
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
- 500 mg/1
Packaging
- 21 CAPSULE in 1 BOTTLE (63629-5739-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7f38a7aa-45bb-4d8c-9595-89fba63cdc96", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308191"], "spl_set_id": ["95eaa9ac-c64a-4f1d-b5a3-66489d5b1edb"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "21 CAPSULE in 1 BOTTLE (63629-5739-1)", "package_ndc": "63629-5739-1", "marketing_start_date": "20250603"}], "brand_name": "Amoxicillin", "product_id": "63629-5739_7f38a7aa-45bb-4d8c-9595-89fba63cdc96", "dosage_form": "CAPSULE", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "63629-5739", "generic_name": "Amoxicillin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "500 mg/1"}], "application_number": "ANDA065271", "marketing_category": "ANDA", "marketing_start_date": "20051109", "listing_expiration_date": "20261231"}