Phloridzin
- Product NDC
- 63083-1535
- 11-digit product format
- 630831535
- Labeler code
- 63083
- Product ID
- 63083-1535_ec59bd4f-c6e7-42af-905a-7c25ee747c84
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Phloridzin
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Professional Complementary Health Formulas
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1984-08-15
- Substance
- PHLORIZIN
- Active strength
- 9 [hp_X]/29.5mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Phloridzin
- Brand name suffix
- 1535
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PHLORIZIN | 9 [hp_X]/29.5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | CU9S17279X |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63083-1535-1 | Phloridzin1535 | 29.5 mL in 1 BOTTLE, DROPPER | LIQUID | 29.5 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63083-1535 | PHLORIDZIN 1535 (PHLORIDZIN) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] | 1 | Current NDC, Legacy NDC, 1 package rows | 20220301_2bfad745-873f-49de-8d6e-9783464aad6c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63083-1535-1 | 63083153501 | 29.5 mL in 1 BOTTLE, DROPPER (63083-1535-1) | 29.5 ml | 1985-08-15 | 0000-00-00 | No | No | Current |