Azurite
- Product NDC
- 63083-8106
- 11-digit product format
- 630838106
- Labeler code
- 63083
- Product ID
- 63083-8106_7ea97a44-435d-4a77-9147-cc8fc82d2869
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Azurite
- 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
- AZURITE
- 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 |
|---|
| 63083-8106 | AZURITE 8106 (AZURITE) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] | 1 | Legacy NDC | 20220216_967ff488-40a0-460f-a51f-3d9c4de4e3f8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63083-8106-2 | 63083810602 | 59 mL in 1 BOTTLE, DROPPER (63083-8106-2) | 59 ml | 1985-08-15 | 0000-00-00 | No | No | Current |