cefixime
Generic: cefixime
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
cefixime
Generic Name
cefixime
Labeler
remedyrepack inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
cefixime 400 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-2749
Product ID
70518-2749_4a8d83f6-006d-5ac4-e063-6294a90abe49
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210574
Listing Expiration
2027-12-31
Marketing Start
2020-05-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705182749
Hyphenated Format
70518-2749
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
cefixime (source: ndc)
Generic Name
cefixime (source: ndc)
Application Number
ANDA210574 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 400 mg/1
Packaging
- 2 CAPSULE in 1 BOTTLE, PLASTIC (70518-2749-2)
- 2 POUCH in 1 BOX (70518-2749-5) / 1 CAPSULE in 1 POUCH (70518-2749-4)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a8d83f6-006d-5ac4-e063-6294a90abe49", "openfda": {"unii": ["97I1C92E55"], "rxcui": ["409823"], "spl_set_id": ["d6718f02-8eea-4c2f-9aa2-65121d9a6e4c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "2 CAPSULE in 1 BOTTLE, PLASTIC (70518-2749-2)", "package_ndc": "70518-2749-2", "marketing_start_date": "20210126"}, {"sample": false, "description": "2 POUCH in 1 BOX (70518-2749-5) / 1 CAPSULE in 1 POUCH (70518-2749-4)", "package_ndc": "70518-2749-5", "marketing_start_date": "20230707"}], "brand_name": "CEFIXIME", "product_id": "70518-2749_4a8d83f6-006d-5ac4-e063-6294a90abe49", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "70518-2749", "generic_name": "CEFIXIME", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CEFIXIME", "active_ingredients": [{"name": "CEFIXIME", "strength": "400 mg/1"}], "application_number": "ANDA210574", "marketing_category": "ANDA", "marketing_start_date": "20200521", "listing_expiration_date": "20271231"}