Pulmo Tartarus 6/8
- Product NDC
- 48951-8092
- 11-digit product format
- 489518092
- Labeler code
- 48951
- Product ID
- 48951-8092_5a995aa4-0b43-c5e0-e063-6294a90a5e42
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pulmo Tartarus 6/8
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- SUS SCROFA LUNG; ANTIMONY POTASSIUM TARTRATE
- Active strength
- 6; 8 [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pulmo Tartarus 6/8
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SUS SCROFA LUNG | 6 [hp_X]/mL |
| ANTIMONY POTASSIUM TARTRATE | 8 [hp_X]/mL |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-8092-1 | Pulmo Tartarus 6/8 | 10 in 1 BOX | LIQUID | 10 | | 4 |
| 48951-8092-1 | Pulmo Tartarus 6/8 | 1 mL in 1 AMPULE | LIQUID | 1 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-8092 | PULMO TARTARUS 6/8 LIQUID [URIEL PHARMACY INC.] | 4 | Current NDC, Legacy NDC, 2 package rows | 20240113_b66a7940-d758-43b7-b962-7bbc7a041a30.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-8092-1 | 48951809201 | 10 AMPULE in 1 BOX (48951-8092-1) / 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | 0000-00-00 | No | No | Current |