Cortisonum 30X
- Product NDC
- 48951-3286
- 11-digit product format
- 489513286
- Labeler code
- 48951
- Product ID
- 48951-3286_5e384044-a941-9a4f-e063-6394a90ab5c6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cortisonum 30X
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- CORTISONE
- Active strength
- 30 [hp_X]/mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- 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
- Cortisonum 30X
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CORTISONE | 30 [hp_X]/mL |
DailyMed Product Concepts#
DailyMed Socrata Ingredients#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-3286-1 | 48951328601 | 10 AMPULE in 1 BOX (48951-3286-1) / 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | No | No | Current |