Olopatadine
- Product NDC
- 55545-1009
- 11-digit product format
- 555451009
- Labeler code
- 55545
- Product ID
- 55545-1009_94785705-19ff-c548-e053-2995a90ab562
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olopatadine
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- FDC Limited
- Application
- ANDA209282
- Marketing category
- ANDA
- Marketing start
- 2020-03-15
- 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 Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record