TIMOLOL MALEATE
- Product NDC
- 70518-2353
- 11-digit product format
- 705182353
- Labeler code
- 70518
- Product ID
- 70518-2353_b970585c-7734-1547-e053-2a95a90afe85
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- timolol maleate
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA074746
- Marketing category
- ANDA
- Marketing start
- 2019-10-08
- 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
- 2022-12-31
- 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 |
|---|
| 70518-2353-0 | 70518235300 | 1 BOTTLE, DROPPER in 1 CARTON (70518-2353-0) > 5 mL in 1 BOTTLE, DROPPER | 2019-10-08 | 0000-00-00 | No | No | Current |