Ketotifen Fumarate
- Product NDC
- 70677-0052
- 11-digit product format
- 706770052
- Labeler code
- 70677
- Product ID
- 70677-0052_463cf8fa-9f84-62a4-8a27-ceea84ad6c88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ketotifen Fumarate
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA077354
- Marketing category
- ANDA
- Marketing start
- 2019-06-18
- Marketing end
- 2022-10-17
- Substance
- KETOTIFEN FUMARATE
- Active strength
- 0 mg/mL
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 70677-0052-1 | 70677005201 | 1 BOTTLE, PLASTIC in 1 CARTON (70677-0052-1) > 5 mL in 1 BOTTLE, PLASTIC | 2019-06-18 | 2022-10-17 | No | No | Current |