OLOPATADINE HYDROCHLORIDE
- Product NDC
- 51407-938
- 11-digit product format
- 514070938
- Labeler code
- 51407
- Product ID
- 51407-938_50b02d58-dd74-6d0a-e063-6294a90a28fd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Olopatadine Hydrochloride ophthalmic
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA200810
- Marketing category
- ANDA
- Marketing start
- 2017-06-28
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- OLOPATADINE HYDROCHLORIDE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OLOPATADINE HYDROCHLORIDE | 1 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2XG66W44KF |
| Rxcui | 1111339 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51407-938-05 | OLOPATADINE HYDROCHLORIDE | 5 mL in 1 BOTTLE, PLASTIC | SOLUTION | 5 | | 1 |
| 51407-938-05 | OLOPATADINE HYDROCHLORIDE | 1 in 1 CARTON | SOLUTION | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 51407-938-05 | 51407093805 | 1 BOTTLE, PLASTIC in 1 CARTON (51407-938-05) / 5 mL in 1 BOTTLE, PLASTIC | 2026-03-03 | No | No | Current |