cromolyn sodium
Generic: cromolyn sodium
Labeler: micro labs limitedDrug Facts
Product Profile
Brand Name
cromolyn sodium
Generic Name
cromolyn sodium
Labeler
micro labs limited
Dosage Form
SOLUTION, CONCENTRATE
Routes
Active Ingredients
cromolyn sodium 100 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
42571-132
Product ID
42571-132_22ffea9c-cd39-22dd-e063-6394a90aae4b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202745
Listing Expiration
2026-12-31
Marketing Start
2013-05-04
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42571132
Hyphenated Format
42571-132
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
cromolyn sodium (source: ndc)
Generic Name
cromolyn sodium (source: ndc)
Application Number
ANDA202745 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/5mL
Packaging
- 96 CARTON in 1 CARTON (42571-132-52) / 1 TRAY in 1 CARTON / 8 AMPULE in 1 TRAY / 5 mL in 1 AMPULE (42571-132-21)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "22ffea9c-cd39-22dd-e063-6394a90aae4b", "openfda": {"unii": ["Q2WXR1I0PK"], "rxcui": ["831261"], "spl_set_id": ["93f80edb-3b38-423e-8cd6-5b5cb4393ec2"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "96 CARTON in 1 CARTON (42571-132-52) / 1 TRAY in 1 CARTON / 8 AMPULE in 1 TRAY / 5 mL in 1 AMPULE (42571-132-21)", "package_ndc": "42571-132-52", "marketing_start_date": "20130504"}], "brand_name": "CROMOLYN SODIUM", "product_id": "42571-132_22ffea9c-cd39-22dd-e063-6394a90aae4b", "dosage_form": "SOLUTION, CONCENTRATE", "pharm_class": ["Decreased Histamine Release [PE]", "Mast Cell Stabilizer [EPC]"], "product_ndc": "42571-132", "generic_name": "Cromolyn sodium", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CROMOLYN SODIUM", "active_ingredients": [{"name": "CROMOLYN SODIUM", "strength": "100 mg/5mL"}], "application_number": "ANDA202745", "marketing_category": "ANDA", "marketing_start_date": "20130504", "listing_expiration_date": "20261231"}