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#