Ferrum Quartz
- Product NDC
- 48951-4197
- 11-digit product format
- 489514197
- Labeler code
- 48951
- Product ID
- 48951-4197_3b5350ed-8f2f-6acb-e063-6394a90a52ab
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ferrum Quartz
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Uriel Pharmacy, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2023-03-30
- Substance
- FERROUS SULFATE; SULFUR
- Active strength
- 1; 1 [hp_X]/1; [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ferrum Quartz
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FERROUS SULFATE | 1 [hp_X]/1 |
| SULFUR | 1 [hp_X]/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 39R4TAN1VT, 70FD1KFU70 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-4197-4 | Ferrum Quartz | 250 in 1 BOTTLE, GLASS | TABLET | 250 | | 4 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-4197-4 | 48951419704 | 250 TABLET in 1 BOTTLE, GLASS (48951-4197-4) | 250 tablet | 2023-03-30 | No | No | Historical |