Darby
- Product NDC
- 66467-3760
- 11-digit product format
- 664673760
- Labeler code
- 66467
- Product ID
- 66467-3760_b60cefef-d19c-66cb-e053-2995a90aa01b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- AEROSOL, FOAM
- Route
- DENTAL
- Labeler
- Darby Dental Supply, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2012-01-31
- Marketing end
- 2021-11-30
- Substance
- SODIUM FLUORIDE
- Active strength
- 0 g/g
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.
Dataset, Scope, Product NDC table| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|
| excluded product | product | 66467-3760 | | D | Discontinued by firm | | 2026-07-31 |
| excluded package | package | 66467-3760 | 66467-3760-1 | D | Discontinued by firm | | 2026-07-31 |
DailyMed Socrata Ingredients#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66467-3760-1 | 66467376001 | 125 g in 1 BOTTLE, SPRAY (66467-3760-1) | 125 g | 2012-01-31 | 2021-11-30 | No | No | Current |