cromolyn sodium
Generic: cromolyn sodium
Labeler: rising pharma holdings, inc.Drug Facts
Product Profile
Brand Name
cromolyn sodium
Generic Name
cromolyn sodium
Labeler
rising pharma holdings, inc.
Dosage Form
SOLUTION, CONCENTRATE
Routes
Active Ingredients
cromolyn sodium 100 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
16571-600
Product ID
16571-600_ca2c72ae-db00-4694-9fd0-d4b6b45f8108
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202583
Listing Expiration
2026-12-31
Marketing Start
2011-12-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
16571600
Hyphenated Format
16571-600
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
ANDA202583 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/5mL
Packaging
- 12 POUCH in 1 CARTON (16571-600-96) / 8 AMPULE in 1 POUCH / 5 mL in 1 AMPULE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ca2c72ae-db00-4694-9fd0-d4b6b45f8108", "openfda": {"unii": ["Q2WXR1I0PK"], "rxcui": ["831261"], "spl_set_id": ["61c9cb85-129e-4490-b5f7-357307fcecbf"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 POUCH in 1 CARTON (16571-600-96) / 8 AMPULE in 1 POUCH / 5 mL in 1 AMPULE", "package_ndc": "16571-600-96", "marketing_start_date": "20111205"}], "brand_name": "CROMOLYN SODIUM", "product_id": "16571-600_ca2c72ae-db00-4694-9fd0-d4b6b45f8108", "dosage_form": "SOLUTION, CONCENTRATE", "pharm_class": ["Decreased Histamine Release [PE]", "Mast Cell Stabilizer [EPC]"], "product_ndc": "16571-600", "generic_name": "CROMOLYN SODIUM", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CROMOLYN SODIUM", "active_ingredients": [{"name": "CROMOLYN SODIUM", "strength": "100 mg/5mL"}], "application_number": "ANDA202583", "marketing_category": "ANDA", "marketing_start_date": "20111205", "listing_expiration_date": "20261231"}