Mercurius 10/20/30 Special Order
- Product NDC
- 48951-7136
- 11-digit product format
- 489517136
- Labeler code
- 48951
- Product ID
- 48951-7136_78d8ccb3-cce6-4afd-8b8b-70ddc078b2ef
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Mercurius 10/20/30 Special Order
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- MERCURY
- Active strength
- 10 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-7136-3 | Mercurius 10/20/30 Special Order | 60 mL in 1 BOTTLE, DROPPER | LIQUID | 60 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-7136 | MERCURIUS 10/20/30 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.] | 1 | Legacy NDC, 1 package rows | 20141204_e95cb934-24ff-415e-90a8-65ecb01a02e4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 48951-7136-3 | 48951713603 | 60 mL in 1 BOTTLE, DROPPER | 60 ml | Historical |