amoxicillin

Generic: amoxicillin

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amoxicillin
Generic Name amoxicillin
Labeler remedyrepack inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

amoxicillin 250 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2188
Product ID 70518-2188_49db778f-96e6-c177-e063-6294a90a1c34
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA064076
Listing Expiration 2027-12-31
Marketing Start 2019-07-09

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705182188
Hyphenated Format 70518-2188

Supplemental Identifiers

RxCUI
308182
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 ANDA064076 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BLISTER PACK (70518-2188-0)
source: ndc

Packages (1)

70518-2188-0 30 CAPSULE in 1 BLISTER PACK (70518-2188-0)

Ingredients (1)

amoxicillin (250 mg/1)

Linked Drug Pages (1)

Amoxicillin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49db778f-96e6-c177-e063-6294a90a1c34", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308182"], "spl_set_id": ["bb95fd06-f200-4de3-bfae-84d642d8e0f3"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-2188-0)", "package_ndc": "70518-2188-0", "marketing_start_date": "20190709"}], "brand_name": "Amoxicillin", "product_id": "70518-2188_49db778f-96e6-c177-e063-6294a90a1c34", "dosage_form": "CAPSULE", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "70518-2188", "generic_name": "Amoxicillin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "250 mg/1"}], "application_number": "ANDA064076", "marketing_category": "ANDA", "marketing_start_date": "20190709", "listing_expiration_date": "20271231"}