Nedocromil Sodium
- Product NDC
- 17478-066
- 11-digit product format
- 174780066
- Labeler code
- 17478
- Product ID
- 17478-066_dfe345fa-029b-49c4-8205-26f3b7d474c8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nedocromil Sodium
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Akorn
- Application
- ANDA090638
- Marketing category
- ANDA
- Marketing start
- 2012-09-10
- Marketing end
- 0000-00-00
- Substance
- NEDOCROMIL SODIUM
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Decreased Histamine Release [PE], Mast Cell Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-066-10 | 17478006610 | 1 BOTTLE, DROPPER in 1 CARTON (17478-066-10) > 5 mL in 1 BOTTLE, DROPPER | 2012-09-10 | 0000-00-00 | No | No | Current |