amoxicillin

Generic: amoxicillin

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amoxicillin
Generic Name amoxicillin
Labeler nucare pharmaceuticals,inc.
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

amoxicillin 250 mg/5mL

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-2364
Product ID 68071-2364_4b354727-eaee-119f-e063-6394a90afd77
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065322
Listing Expiration 2027-12-31
Marketing Start 2006-06-19

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680712364
Hyphenated Format 68071-2364

Supplemental Identifiers

RxCUI
239191
UPC
0368071236484
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 ANDA065322 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/5mL
source: ndc
Packaging
  • 80 mL in 1 BOTTLE (68071-2364-8)
source: ndc

Packages (1)

68071-2364-8 80 mL in 1 BOTTLE (68071-2364-8)

Ingredients (1)

amoxicillin (250 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": "4b354727-eaee-119f-e063-6394a90afd77", "openfda": {"upc": ["0368071236484"], "unii": ["804826J2HU"], "rxcui": ["239191"], "spl_set_id": ["bd46de4c-4571-ba9a-e053-2a95a90a792d"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "80 mL in 1 BOTTLE (68071-2364-8)", "package_ndc": "68071-2364-8", "marketing_start_date": "20210311"}], "brand_name": "Amoxicillin", "product_id": "68071-2364_4b354727-eaee-119f-e063-6394a90afd77", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "68071-2364", "generic_name": "Amoxicillin", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "250 mg/5mL"}], "application_number": "ANDA065322", "marketing_category": "ANDA", "marketing_start_date": "20060619", "listing_expiration_date": "20271231"}