Lachesis Belladonna
- Product NDC
- 48951-6013
- Requested package NDC
- 48951-6013-3
- 11-digit product format
- 489516013
- Labeler code
- 48951
- Product ID
- 48951-6013_6ad48609-b130-ecf3-e053-2991aa0ad704
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lachesis Belladonna
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- MERCURIALIS PERENNIS; ATROPA BELLADONNA; CALCIUM SULFIDE; LACHESIS MUTA VENOM
- Active strength
- 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-6013-3 | Lachesis Belladonna | 60 mL in 1 BOTTLE, DROPPER | LIQUID | 60 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-6013 | LACHESIS BELLADONNA LIQUID [URIEL PHARMACY INC.] | 3 | Legacy NDC, 1 package rows | 20180427_cd4d2eae-73f8-4168-b1b6-abf43d9326e9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-6013-3 | 48951601303 | 60 mL in 1 BOTTLE, DROPPER (48951-6013-3) | 60 ml | 2009-09-01 | 0000-00-00 | No | No | Current |