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 68071-3678
Product ID 68071-3678_2177c2a1-7295-5971-e063-6394a90a9282
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065322
Listing Expiration 2026-12-31
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 680713678
Hyphenated Format 68071-3678

Supplemental Identifiers

RxCUI
239191
UPC
0368071367812
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
  • 100 mL in 1 BOTTLE (68071-3678-1)
source: ndc

Packages (1)

68071-3678-1 100 mL in 1 BOTTLE (68071-3678-1)

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": "2177c2a1-7295-5971-e063-6394a90a9282", "openfda": {"upc": ["0368071367812"], "unii": ["804826J2HU"], "rxcui": ["239191"], "spl_set_id": ["2177c68d-2884-ce70-e063-6294a90aa267"], "manufacturer_name": ["NuCare Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (68071-3678-1)", "package_ndc": "68071-3678-1", "marketing_start_date": "20240906"}], "brand_name": "Amoxicillin", "product_id": "68071-3678_2177c2a1-7295-5971-e063-6394a90a9282", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "68071-3678", "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": "20261231"}