Vanilla Planifolia
- Product NDC
- 63545-688
- 11-digit product format
- 635450688
- Labeler code
- 63545
- Product ID
- 63545-688_4ec9b6dd-d634-3cc1-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Vanilla Planifolia
- Dosage form
- PELLET
- Route
- BUCCAL; ORAL; SUBLINGUAL
- Labeler
- Hahnemann Laboratories, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2017-05-05
- Marketing end
- 0000-00-00
- Substance
- VANILLA PLANIFOLIA WHOLE
- Active strength
- 30 [hp_C]/[hp_C]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63545-688-01 | Vanilla Planifolia | 240 [hp_C] in 1 VIAL, GLASS | PELLET | 240 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63545-688 | VANILLA PLANIFOLIA PELLET [HAHNEMANN LABORATORIES, INC.] | 1 | Legacy NDC, 1 package rows | 20170505_4ec9b6dd-d633-3cc1-e054-00144ff88e88.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 63545-688-01 | 63545068801 | 240 [hp_C] in 1 VIAL, GLASS | Historical |