TIMOLOL MALEATE
- Product NDC
- 70518-2354
- 11-digit product format
- 705182354
- Labeler code
- 70518
- Product ID
- 70518-2354_95ffb112-299e-7a31-e053-2995a90abaa7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- timolol maleate
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077259
- Marketing category
- ANDA
- Marketing start
- 2019-10-09
- Marketing end
- 0000-00-00
- Substance
- TIMOLOL MALEATE
- Active strength
- 3 mg/mL
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record