Cromolyn Sodium
- Product NDC
- 50090-3042
- 11-digit product format
- 500903042
- Labeler code
- 50090
- Product ID
- 50090-3042_e5a09b32-2922-4ad9-a56a-9ab2d6d3bb55
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cromolyn Sodium
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- A-S Medication Solutions
- Application
- ANDA074706
- Marketing category
- ANDA
- Marketing start
- 1998-04-29
- Marketing end
- 0000-00-00
- Substance
- CROMOLYN SODIUM
- Active strength
- 40 mg/mL
- Pharmacologic classes
- Decreased Histamine Release [PE],Mast Cell Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3042-0 | 50090304200 | 1 BOTTLE, DROPPER in 1 CARTON (50090-3042-0) > 10 mL in 1 BOTTLE, DROPPER | 2017-06-07 | 0000-00-00 | No | No | Current |