Bambusa Argentum
- Product NDC
- 48951-2007
- 11-digit product format
- 489512007
- Labeler code
- 48951
- Product ID
- 48951-2007_6ce05eb8-7e3e-f063-e053-2a91aa0a7a45
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bambusa 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
- BAMBUSA VULGARIS WHOLE; STACHYS OFFICINALIS; ROSMARINUS OFFICINALIS FLOWERING TOP; FORMICA RUFA; BOS TAURUS INTERVERTEBRAL DISC; SILICON DIOXIDE; SILVER; ARNICA MONTANA
- Active strength
- 6 [hp_X]/1; [hp_X]/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 |
|---|
| 48951-2007-2 | Bambusa Argentum | 1350 in 1 BOTTLE, GLASS | PELLET | 1350 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-2007 | BAMBUSA ARGENTUM PELLET [URIEL PHARMACY INC.] | 2 | Legacy NDC, 1 package rows | 20180523_ad19a274-fe9a-4249-be64-dfc0e0edda62.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-2007-2 | 48951200702 | 1350 PELLET in 1 BOTTLE, GLASS (48951-2007-2) | 1350 pellet | 2009-09-01 | 0000-00-00 | No | No | Current |