Ketotifen Fumarate
- Product NDC
- 50090-2900
- 11-digit product format
- 500902900
- Labeler code
- 50090
- Product ID
- 50090-2900_6e88d166-c147-41ba-ad0d-b195952a057d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ketotifen Fumarate
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- A-S Medication Solutions
- Application
- ANDA077958
- Marketing category
- ANDA
- Marketing start
- 2007-10-01
- Marketing end
- 0000-00-00
- Substance
- KETOTIFEN FUMARATE
- Active strength
- 0 mg/mL
- 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 |
|---|
| 50090-2900-0 | 50090290000 | 1 BOTTLE, DROPPER in 1 CARTON (50090-2900-0) > 5 mL in 1 BOTTLE, DROPPER | 2017-03-03 | 0000-00-00 | No | No | Current |