cipro
Generic: ciprofloxacin
Labeler: bayer healthcare pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
cipro
Generic Name
ciprofloxacin
Labeler
bayer healthcare pharmaceuticals inc.
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
50419-777
Product ID
50419-777_1b112839-6cf0-466a-9188-86fc5b1549f9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA020780
Listing Expiration
2027-12-31
Marketing Start
1997-09-26
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50419777
Hyphenated Format
50419-777
Supplemental Identifiers
RxCUI
UPC
UNII
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
cipro (source: ndc)
Generic Name
ciprofloxacin (source: ndc)
Application Number
NDA020780 (source: ndc)
Routes
source: label
Resolved Composition
Strengths
- 250 mg
- 500 mg
- 5 %
- 250 mg/5 ml
- 10 %
- 500 mg/5 ml
- 5 ml
- 100 ml
- 5000 mg
- 10000 mg
- 2.5 ml
Packaging
- 1 KIT in 1 KIT (50419-777-01) * 100 mL in 1 BOTTLE, GLASS * 100 mL in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "1b112839-6cf0-466a-9188-86fc5b1549f9", "openfda": {"upc": ["0350419754019", "0350419758017"], "unii": ["4BA73M5E37"], "rxcui": ["197511", "205769", "205770", "213224", "213226", "309308", "309309", "309310"], "spl_set_id": ["888dc7f9-ad9c-4c00-8d50-8ddfd9bd27c0"], "manufacturer_name": ["Bayer HealthCare Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (50419-777-01) * 100 mL in 1 BOTTLE, GLASS * 100 mL in 1 BOTTLE, PLASTIC", "package_ndc": "50419-777-01", "marketing_start_date": "19970926"}], "brand_name": "Cipro", "product_id": "50419-777_1b112839-6cf0-466a-9188-86fc5b1549f9", "dosage_form": "KIT", "product_ndc": "50419-777", "generic_name": "ciprofloxacin", "labeler_name": "Bayer HealthCare Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cipro", "application_number": "NDA020780", "marketing_category": "NDA", "marketing_start_date": "19970926", "listing_expiration_date": "20271231"}