alocril
Generic: nedocromil sodium
Labeler: allergan, inc.Drug Facts
Product Profile
Brand Name
alocril
Generic Name
nedocromil sodium
Labeler
allergan, inc.
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
nedocromil sodium 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0023-8842
Product ID
0023-8842_d5f0e9b5-9b78-4dc2-9480-77187ee87df1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA021009
Listing Expiration
2026-12-31
Marketing Start
2000-02-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00238842
Hyphenated Format
0023-8842
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
alocril (source: ndc)
Generic Name
nedocromil sodium (source: ndc)
Application Number
NDA021009 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 1 BOTTLE, DROPPER in 1 CARTON (0023-8842-05) / 5 mL in 1 BOTTLE, DROPPER
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "d5f0e9b5-9b78-4dc2-9480-77187ee87df1", "openfda": {"upc": ["0300238842053"], "unii": ["ET8IF4KS1T"], "rxcui": ["897292", "897294"], "spl_set_id": ["2fe8d7ad-2158-4169-94b0-719ad20242b7"], "manufacturer_name": ["Allergan, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (0023-8842-05) / 5 mL in 1 BOTTLE, DROPPER", "package_ndc": "0023-8842-05", "marketing_start_date": "20000203"}], "brand_name": "ALOCRIL", "product_id": "0023-8842_d5f0e9b5-9b78-4dc2-9480-77187ee87df1", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Decreased Histamine Release [PE]", "Mast Cell Stabilizer [EPC]"], "product_ndc": "0023-8842", "generic_name": "nedocromil sodium", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALOCRIL", "active_ingredients": [{"name": "NEDOCROMIL SODIUM", "strength": "20 mg/mL"}], "application_number": "NDA021009", "marketing_category": "NDA", "marketing_start_date": "20000203", "listing_expiration_date": "20261231"}