Quercus Rubra Glandium
- Product NDC
- 63545-666
- 11-digit product format
- 635450666
- Labeler code
- 63545
- Product ID
- 63545-666_44bdd485-709d-28a1-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Quercus Rubra Glandium
- Dosage form
- PELLET
- Route
- BUCCAL; ORAL; SUBLINGUAL
- Labeler
- Hahnemann Laboratories, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-12-01
- Marketing end
- 0000-00-00
- Substance
- QUERCUS RUBRA 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 |
|---|
| 63545-666-01 | Quercus Rubra Glandium | 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 |
|---|
| 63545-666 | QUERCUS RUBRA GLANDIUM PELLET [HAHNEMANN LABORATORIES, INC.] | 1 | Legacy NDC, 1 package rows | 20161229_44bdd485-709c-28a1-e054-00144ff88e88.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 63545-666-01 | 63545066601 | 240 [hp_C] in 1 VIAL, GLASS | Historical |