amoxicillin

Generic: amoxicillin

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

Drug Facts

Product Profile

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

amoxicillin 125 mg/5mL

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-9949
Product ID 68788-9949_1f544b8d-2ee6-4dc8-8289-9684aaa95119
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065387
Listing Expiration 2027-12-31
Marketing Start 2012-01-12

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687889949
Hyphenated Format 68788-9949

Supplemental Identifiers

RxCUI
239191 313797
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 ANDA065387 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 125 mg/5mL
source: ndc
Packaging
  • 150 mL in 1 BOTTLE (68788-9949-1)
source: ndc

Packages (1)

68788-9949-1 150 mL in 1 BOTTLE (68788-9949-1)

Ingredients (1)

amoxicillin (125 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": "1f544b8d-2ee6-4dc8-8289-9684aaa95119", "openfda": {"unii": ["804826J2HU"], "rxcui": ["239191", "313797"], "spl_set_id": ["88e76bdd-39f2-48c4-91ca-609511afd382"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "150 mL in 1 BOTTLE (68788-9949-1)", "package_ndc": "68788-9949-1", "marketing_start_date": "20120112"}], "brand_name": "Amoxicillin", "product_id": "68788-9949_1f544b8d-2ee6-4dc8-8289-9684aaa95119", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "68788-9949", "generic_name": "Amoxicillin", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "125 mg/5mL"}], "application_number": "ANDA065387", "marketing_category": "ANDA", "marketing_start_date": "20120112", "listing_expiration_date": "20271231"}