carboxymethylcellulose sodium
Generic: carboxymethylcellulose sodium
Labeler: avpakDrug Facts
Product Profile
Brand Name
carboxymethylcellulose sodium
Generic Name
carboxymethylcellulose sodium
Labeler
avpak
Dosage Form
GEL
Routes
Active Ingredients
carboxymethylcellulose sodium 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
50268-065
Product ID
50268-065_47e225fb-3d2e-4f80-e063-6394a90aff85
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M018
Listing Expiration
2027-12-31
Marketing Start
2020-11-18
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50268065
Hyphenated Format
50268-065
Supplemental Identifiers
RxCUI
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
carboxymethylcellulose sodium (source: ndc)
Generic Name
carboxymethylcellulose sodium (source: ndc)
Application Number
M018 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 30 VIAL, SINGLE-USE in 1 CARTON (50268-065-30) / .4 mL in 1 VIAL, SINGLE-USE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "47e225fb-3d2e-4f80-e063-6394a90aff85", "openfda": {"unii": ["K679OBS311"], "rxcui": ["579907"], "spl_set_id": ["b4697319-438e-2ec8-e053-2a95a90abb56"], "manufacturer_name": ["AvPAK"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 VIAL, SINGLE-USE in 1 CARTON (50268-065-30) / .4 mL in 1 VIAL, SINGLE-USE", "package_ndc": "50268-065-30", "marketing_start_date": "20201118"}], "brand_name": "carboxymethylcellulose sodium", "product_id": "50268-065_47e225fb-3d2e-4f80-e063-6394a90aff85", "dosage_form": "GEL", "product_ndc": "50268-065", "generic_name": "carboxymethylcellulose sodium", "labeler_name": "AvPAK", "product_type": "HUMAN OTC DRUG", "brand_name_base": "carboxymethylcellulose sodium", "active_ingredients": [{"name": "CARBOXYMETHYLCELLULOSE SODIUM", "strength": "10 mg/mL"}], "application_number": "M018", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20201118", "listing_expiration_date": "20271231"}