Antimonite Belladonna
- Product NDC
- 48951-1037
- 11-digit product format
- 489511037
- Labeler code
- 48951
- Product ID
- 48951-1037_6983c4f2-0167-ba15-e053-2991aa0a3625
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Antimonite Belladonna
- Dosage form
- POWDER
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- ANTIMONY TRISULFIDE; ATROPA BELLADONNA; MATRICARIA RECUTITA; BISMUTH SUBNITRATE
- Active strength
- 3 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-1037-4 | Antimonite Belladonna | 50 g in 1 BOTTLE, GLASS | POWDER | 50 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-1037 | ANTIMONITE BELLADONNA POWDER [URIEL PHARMACY INC.] | 5 | Legacy NDC, 1 package rows | 20240113_0bc61339-130a-459b-9c61-2a12b5572347.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-1037-4 | 48951103704 | 50 g in 1 BOTTLE, GLASS (48951-1037-4) | 50 g | 2009-09-01 | 0000-00-00 | No | No | Current |