KETOTIFEN FUMARATE
- Product NDC
- 72189-114
- 11-digit product format
- 721890114
- Labeler code
- 72189
- Product ID
- 72189-114_c2d7d12d-4186-6bde-e053-2995a90a538e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- KETOTIFEN FUMARATE
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- DIRECT RX
- Application
- ANDA077354
- Marketing category
- ANDA
- Marketing start
- 2020-06-25
- Marketing end
- 0000-00-00
- Substance
- KETOTIFEN FUMARATE
- Active strength
- 0 mg/mL
- 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 |
|---|
| 72189-114-05 | 72189011405 | 5 mL in 1 BOTTLE, PLASTIC (72189-114-05) | 5 ml | 2020-06-25 | 0000-00-00 | No | No | Current |