Cromolyn Sodium

Product NDC
37205-223
11-digit product format
372050223
Labeler code
37205
Product ID
37205-223_fc05700f-0a6b-4693-a3f4-3211606f660d
Type
HUMAN OTC DRUG
Nonproprietary name
Cromolyn Sodium
Dosage form
SPRAY, METERED
Route
NASAL
Labeler
Cardinal Health
Application
ANDA075702
Marketing category
ANDA
Marketing start
2010-07-03
Marketing end
0000-00-00
Substance
CROMOLYN SODIUM
Active strength
5 mg/mL
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
37205-223-612025-04-08C16284748780-19d75b9d0-05aa-f424-e053-dadaa90a57cefc05700f-0a6b-4693-a3f4-3211606f660d
37205-223-612020-01-31C16284748780-19d75b9d0-05aa-f424-e053-dadaa90a57cefc05700f-0a6b-4693-a3f4-3211606f660d

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
37205-223-61ML - Milliliter37205-22302435f4b-26dc-4d6c-a8b4-ad17379e83f312012-07-24