Timoptic in Ocudose
- Product NDC
- 69918-602
- 11-digit product format
- 699180602
- Labeler code
- 69918
- Product ID
- 69918-602_1a4d5b53-65eb-4b2d-9ded-526f8ad9b51d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Timolol Maleate
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- Amring Pharmaceuticals Inc.
- Application
- ANDA212592
- Marketing category
- ANDA
- Marketing start
- 2022-02-26
- 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 |
|---|
| 69918-602 | TIMOPTIC IN OCUDOSE (TIMOLOL MALEATE) SOLUTION [NORDIC PHARMA, INC.] | 3 | Legacy NDC | 20250323_16323b0e-78ae-40e5-be93-04f698dd672b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69918-602-60 | 69918060260 | 60 POUCH in 1 CARTON (69918-602-60) > 10 CONTAINER in 1 POUCH > .3 mL in 1 CONTAINER | 60 pouch | 2022-02-26 | 0000-00-00 | No | No | Current |