Olopatadine Hydrochloride
- Product NDC
- 69367-233
- 11-digit product format
- 693670233
- Labeler code
- 69367
- Product ID
- 69367-233_c729941c-bc49-4754-83b8-33ab7bbebf09
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olopatadine Hydrochloride
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Westminster Pharmaceuticals, LLC
- Application
- ANDA203152
- Marketing category
- ANDA
- Marketing start
- 2019-09-19
- Marketing end
- 2022-05-02
- 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
- 0000-00-00
- 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 |
|---|
| 69367-233-05 | 69367023305 | 5 mL in 1 BOTTLE, DROPPER (69367-233-05) | 5 ml | 2019-09-19 | 0000-00-00 | No | No | Current |