Denti-Care Denti-Pro
- Product NDC
- 64778-0216
- 11-digit product format
- 647780216
- Labeler code
- 64778
- Product ID
- 64778-0216_b9e45d8d-dd41-f7f3-e053-2995a90a7973
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- GEL
- Route
- DENTAL
- Labeler
- AMD Medicom Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1999-10-01
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 0 g/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 64778-0216-3 | 64778021603 | 12 BOTTLE, PLASTIC in 1 CASE (64778-0216-3) > 480 mL in 1 BOTTLE, PLASTIC (64778-0216-1) | 2017-12-01 | 0000-00-00 | No | No | Current |