Apis Eucalyptus Special Order
- Product NDC
- 48951-1052
- 11-digit product format
- 489511052
- Labeler code
- 48951
- Product ID
- 48951-1052_9c0596f7-690f-4e54-8db7-bbcc0292f90b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Apis Eucalyptus Special Order
- Dosage form
- POWDER
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- APIS MELLIFERA; ATROPA BELLADONNA; EUCALYPTUS GUM
- Active strength
- 3 [hp_X]/g; [hp_X]/g; [hp_X]/g
- 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 |
|---|
| 48951-1052-4 | Apis Eucalyptus Special Order | 50 g in 1 BOTTLE, GLASS | POWDER | 50 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-1052 | APIS EUCALYPTUS SPECIAL ORDER POWDER [URIEL PHARMACY INC.] | 1 | Legacy NDC, 1 package rows | 20141122_1e1040c2-7be5-47de-952c-df40f631f79e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 48951-1052-4 | 48951105204 | 50 g in 1 BOTTLE, GLASS | 50 g | Historical |