Betula Argentum
- Product NDC
- 48951-2064
- 11-digit product format
- 489512064
- Labeler code
- 48951
- Product ID
- 48951-2064_6d86672e-b53e-2007-e053-2a91aa0ada70
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Betula Argentum
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- BETULA PUBESCENS BARK; BETULA PUBESCENS LEAF; APIS MELLIFERA; FORMICA RUFA; SILVER; ARNICA MONTANA
- Active strength
- 1 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-2064-2 | Betula Argentum | 1350 in 1 BOTTLE, GLASS | PELLET | 1350 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-2064 | BETULA ARGENTUM PELLET [URIEL PHARMACY INC.] | 3 | Legacy NDC, 1 package rows | 20180601_0d697558-af48-4173-9603-fc2c4bb9915f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-2064-2 | 48951206402 | 1350 PELLET in 1 BOTTLE, GLASS (48951-2064-2) | 1350 pellet | 2009-09-01 | 0000-00-00 | No | No | Current |