Timolol Maleate
- Product NDC
- 24208-818
- 11-digit product format
- 242080818
- Labeler code
- 24208
- Product ID
- 24208-818_b2a3e6e1-d01c-4d14-85ac-41905306d769
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Timolol Maleate
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- Bausch & Lomb Incorporated
- Application
- NDA020330
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2018-02-14
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24208-818 | TIMOLOL MALEATE SOLUTION [BAUSCH & LOMB INCORPORATED] | 2 | Legacy NDC | 20210605_1f886442-2781-4be4-b20d-d22c2c209790.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 24208-818-25 | 24208081825 | 1 BOTTLE, DISPENSING in 1 CARTON (24208-818-25) > 5 mL in 1 BOTTLE, DISPENSING | 2018-02-14 | 0000-00-00 | No | No | Current |