Cromolyn Sodium Inhalation Solution
- Product NDC
- 60940-032
- 11-digit product format
- 609400032
- Labeler code
- 60940
- Product ID
- 60940-032_d0d730f8-3407-9f18-e053-2995a90a34c7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cromolyn Sodium
- Dosage form
- SOLUTION
- Route
- INTRABRONCHIAL
- Labeler
- Holopack Verpackungstechnik GmbH
- Application
- ANDA075437
- Marketing category
- ANDA
- Marketing start
- 2021-11-30
- Marketing end
- 0000-00-00
- Substance
- CROMOLYN SODIUM
- Active strength
- 20 mg/2mL
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60940-032-01 | 60940003201 | 5 POUCH in 1 CARTON (60940-032-01) > 6 VIAL, SINGLE-DOSE in 1 POUCH > 2 mL in 1 VIAL, SINGLE-DOSE | 5 pouch | 2021-11-30 | 0000-00-00 | No | No | Current |