GRAPHITE
- Product NDC
- 10191-1794
- 11-digit product format
- 101911794
- Labeler code
- 10191
- Product ID
- 10191-1794_d32457a2-8cff-4c4b-9677-cdd4349cf15a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- GRAPHITES
- Dosage form
- PELLET
- Route
- SUBLINGUAL
- Labeler
- REMEDY MAKERS
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2004-08-26
- Marketing end
- 0000-00-00
- Substance
- GRAPHITE
- Active strength
- 9 [hp_C]/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 10191-1794-2 | GRAPHITE | 142 in 1 VIAL, GLASS | PELLET | 142 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10191-1794 | GRAPHITE (GRAPHITES) PELLET [REMEDY MAKERS] | 1 | Legacy NDC, 1 package rows | 20111018_ed5d75bc-686f-4af0-ae76-09ba06e8adfd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10191-1794-2 | 10191179402 | 142 in 1 VIAL, GLASS | Historical |