Lapis Lazuli
- Product NDC
- 63083-8129
- 11-digit product format
- 630838129
- Labeler code
- 63083
- Product ID
- 63083-8129_a7fefc97-7a5e-466a-b901-b884909f2ce1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lapis Lazuli
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Professional Complementary Health Formulas
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1984-08-15
- Marketing end
- 0000-00-00
- Substance
- CALCIUM HEXAFLUOROSILICATE
- Active strength
- 6 [hp_X]/59mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63083-8129 | LAPIS LAZULI 8129 (LAPIS LAZULI) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] | 1 | Legacy NDC | 20220217_5483fdde-3f76-4d4e-88fb-fff160a294ea.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63083-8129-2 | 63083812902 | 59 mL in 1 BOTTLE, DROPPER (63083-8129-2) | 59 ml | 1985-08-15 | 0000-00-00 | No | No | Current |