cefprozil
Generic: cefprozil
Labeler: northstar rx llcDrug Facts
Product Profile
Brand Name
cefprozil
Generic Name
cefprozil
Labeler
northstar rx llc
Dosage Form
POWDER, FOR SUSPENSION
Routes
Active Ingredients
cefprozil 125 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
16714-396
Product ID
16714-396_f8a7ccea-370c-4afe-92f2-2f4bcc925669
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065381
Listing Expiration
2026-12-31
Marketing Start
2007-01-30
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
16714396
Hyphenated Format
16714-396
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
cefprozil (source: ndc)
Generic Name
cefprozil (source: ndc)
Application Number
ANDA065381 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 125 mg/5mL
Packaging
- 75 mL in 1 BOTTLE (16714-396-02)
- 100 mL in 1 BOTTLE (16714-396-03)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f8a7ccea-370c-4afe-92f2-2f4bcc925669", "openfda": {"nui": ["N0000175488", "M0003827"], "upc": ["0316714396019", "0316714397016"], "unii": ["4W0459ZA4V"], "rxcui": ["309080", "309081"], "spl_set_id": ["8e3943b5-8c30-4c81-bcfa-aeaaa1d75fb4"], "pharm_class_cs": ["Cephalosporins [CS]"], "pharm_class_epc": ["Cephalosporin Antibacterial [EPC]"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "75 mL in 1 BOTTLE (16714-396-02)", "package_ndc": "16714-396-02", "marketing_start_date": "20070130"}, {"sample": false, "description": "100 mL in 1 BOTTLE (16714-396-03)", "package_ndc": "16714-396-03", "marketing_start_date": "20070130"}], "brand_name": "Cefprozil", "product_id": "16714-396_f8a7ccea-370c-4afe-92f2-2f4bcc925669", "dosage_form": "POWDER, FOR SUSPENSION", "product_ndc": "16714-396", "generic_name": "Cefprozil", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefprozil", "active_ingredients": [{"name": "CEFPROZIL", "strength": "125 mg/5mL"}], "application_number": "ANDA065381", "marketing_category": "ANDA", "marketing_start_date": "20070130", "listing_expiration_date": "20261231"}