Olopatadine
- Product NDC
- 51407-499
- 11-digit product format
- 514070499
- Labeler code
- 51407
- Product ID
- 51407-499_ec0caf45-cc77-b4c1-e053-2a95a90a1abd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Olopatadine Hydrochloride
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA204532
- Marketing category
- ANDA
- Marketing start
- 2017-01-10
- Marketing end
- 0000-00-00
- Substance
- OLOPATADINE HYDROCHLORIDE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Decreased Histamine Release [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Histamine-1 Receptor Inhibitor [EPC], Mast Cell Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 51407-499-05 | 51407049905 | 1 BOTTLE, DROPPER in 1 CARTON (51407-499-05) > 5 mL in 1 BOTTLE, DROPPER | 2021-09-09 | 0000-00-00 | No | No | Current |