Crataegus e fol. et fructus 2 Special Order
- Product NDC
- 48951-3165
- 11-digit product format
- 489513165
- Labeler code
- 48951
- Product ID
- 48951-3165_093127f0-1a9a-4064-ad62-578bdf933965
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Crataegus e fol. et fructus 2 Special Order
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- HAWTHORN LEAF WITH FLOWER
- Active strength
- 2 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 48951-3165-1 | Crataegus e fol. et fructus 2 Special Order | 10 in 1 BOX | LIQUID | 10 | | 1 |
| 48951-3165-1 | Crataegus e fol. et fructus 2 Special Order | 1 mL in 1 AMPULE | LIQUID | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-3165 | CRATAEGUS E FOL. ET FRUCTUS 2 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.] | 1 | Legacy NDC, 2 package rows | 20141007_6a6bd581-1068-4028-b8af-849dfd71829d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 48951-3165-1 | 48951316501 | 10 in 1 BOX | Historical |