NDC 0065-0245 - Betoptic
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 0065-0245
- Package NDCs from labels
- 0065-0245-20, 0065-0245-05, 0065-0245-10, 0065-0245-15
- Manufacturer
- Alcon
- Effective date
- 2006-10-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Betoptic - Alcon | Alcon | 2006-10-30 | Human Prescription Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0065-0245-05 | Betoptic | 5 mL in 1 BOTTLE, PLASTIC | SOLUTION/ DROPS | 5 | 1 | |
| 0065-0245-10 | Betoptic | 10 mL in 1 BOTTLE, PLASTIC | SOLUTION/ DROPS | 10 | 1 | |
| 0065-0245-15 | Betoptic | 15 mL in 1 BOTTLE, PLASTIC | SOLUTION/ DROPS | 15 | 1 | |
| 0065-0245-20 | Betoptic | 2.5 mL in 1 BOTTLE, PLASTIC | SOLUTION/ DROPS | 2.5 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| betaxolol hydrochloride | ACTIVE INGREDIENT | 6X97D2XT0O | BETOPTIC (BETAXOLOL HYDROCHLORIDE) SOLUTION/ DROPS [ALCON] | 1 | |
| betaxolol | ACTIVE MOIETY | O0ZR1R6RZ2 | BETOPTIC (BETAXOLOL HYDROCHLORIDE) SOLUTION/ DROPS [ALCON] | 1 | |
| benzalkonium chloride | INACTIVE INGREDIENT | BETOPTIC (BETAXOLOL HYDROCHLORIDE) SOLUTION/ DROPS [ALCON] | 1 | ||
| edetate disodium | INACTIVE INGREDIENT | 7FLD91C86K | BETOPTIC (BETAXOLOL HYDROCHLORIDE) SOLUTION/ DROPS [ALCON] | 1 | |
| hydrochloric acid and/or sodium hydroxide | INACTIVE INGREDIENT | BETOPTIC (BETAXOLOL HYDROCHLORIDE) SOLUTION/ DROPS [ALCON] | 1 | ||
| sodium chloride | INACTIVE INGREDIENT | 451W47IQ8X | BETOPTIC (BETAXOLOL HYDROCHLORIDE) SOLUTION/ DROPS [ALCON] | 1 | |
| water | INACTIVE INGREDIENT | 059QF0KO0R | BETOPTIC (BETAXOLOL HYDROCHLORIDE) SOLUTION/ DROPS [ALCON] | 1 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Betaxolol Hydrochloride | BETAXOLOL HYDROCHLORIDE | Sandoz Inc | a73519d5-546c-4377-92ed-0d4be2685d60 | 2023-10-31 | Warnings, Adverse reactions | 308720 |
| 0586E0A0-1962-3D4A-1A09-A543AF931CDF | 31b9b263-11fd-4495-83dd-ababf0d70e9e | 2006-10-30 | Warnings, Adverse reactions | 0586E0A0-1962-3D4A-1A09-A543AF931CDF 31b9b263-11fd-4495-83dd-ababf0d70e9e |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.