Ananassa Resina
- Product NDC
- 48951-1032
- 11-digit product format
- 489511032
- Labeler code
- 48951
- Product ID
- 48951-1032_5a38f8f5-eb7d-4ab6-ae4c-9848ef868898
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ananassa Resina
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- PINEAPPLE; COLLOIDAL SILICON DIOXIDE; LARIX DECIDUA RESIN
- Active strength
- 30 [hp_X]/mL; [hp_X]/mL; [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 |
|---|
| 48951-1032-1 | Ananassa Resina | 1 mL in 1 AMPULE | LIQUID | 1 | | 1 |
| 48951-1032-1 | Ananassa Resina | 10 in 1 BOX | LIQUID | 10 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-1032 | ANANASSA RESINA LIQUID [URIEL PHARMACY INC.] | 1 | Legacy NDC, 2 package rows | 20140825_72f1c0f9-ca75-4cdf-a34d-ba80dc8fbe69.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 48951-1032-1 | 48951103201 | 1 mL in 1 AMPULE | 1 ml | Historical |