OLOPATADINE HYDROCHLORIDE
- Product NDC
- 42571-152
- 11-digit product format
- 425710152
- Labeler code
- 42571
- Product ID
- 42571-152_a8bc2472-3d0d-4fa1-e053-2a95a90a963a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OLOPATADINE HYDROCHLORIDE
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Micro Labs Limited
- Application
- ANDA204620
- Marketing category
- ANDA
- Marketing start
- 2020-12-16
- Marketing end
- 0000-00-00
- Substance
- OLOPATADINE HYDROCHLORIDE
- Active strength
- 2 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42571-152-35 | 42571015235 | 1 BOTTLE in 1 CARTON (42571-152-35) > 2.5 mL in 1 BOTTLE | 1 bottle | 2020-12-16 | 0000-00-00 | No | No | Current |