ACTIVATED CHARCOAL
- Product NDC
- 51662-1200
- 11-digit product format
- 516621200
- Labeler code
- 51662
- Product ID
- 51662-1200_9ef30198-d1e0-3fa8-e053-2995a90ae895
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ACTIVATED CHARCOAL
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2018-12-22
- Marketing end
- 0000-00-00
- Substance
- ACTIVATED CHARCOAL
- Active strength
- 208 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 51662-1200-1 | ACTIVATED CHARCOAL | 129 mL in 1 TUBE | SUSPENSION | 129 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51662-1200 | ACTIVATED CHARCOAL SUSPENSION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] | 3 | Legacy NDC, 1 package rows | 20200220_7da3506f-2799-434c-e053-2a91aa0adabb.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51662-1200-1 | 51662120001 | 129 mL in 1 TUBE (51662-1200-1) | 129 ml | 2018-12-22 | 0000-00-00 | No | No | Current |