cromolyn sodium

Generic: cromolyn sodium

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cromolyn sodium
Generic Name cromolyn sodium
Labeler rising pharma holdings, inc.
Dosage Form SOLUTION, CONCENTRATE
Routes
ORAL
Active Ingredients

cromolyn sodium 100 mg/5mL

Manufacturer
Rising Pharma Holdings, Inc.

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
decreased histamine release [pe] mast cell stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 16571600
Hyphenated Format 16571-600

Supplemental Identifiers

RxCUI
831261
UNII
Q2WXR1I0PK

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/5mL
source: ndc
Packaging
  • 12 POUCH in 1 CARTON (16571-600-96) / 8 AMPULE in 1 POUCH / 5 mL in 1 AMPULE
source: ndc

Packages (1)

Ingredients (1)

cromolyn sodium (100 mg/5mL)

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"}