Actidose
- Product NDC
- 0574-0120
- 11-digit product format
- 005740120
- Labeler code
- 0574
- Product ID
- 0574-0120_8a99fab9-1fa2-43e4-a61b-4f876d39116c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Activated Charcoal
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Padagis US LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1983-10-01
- Marketing end
- 2022-01-31
- Substance
- ACTIVATED CHARCOAL
- Active strength
- 208 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0574-0120-04 | 00574012004 | 120 mL in 1 BOTTLE (0574-0120-04) | 120 ml | 1983-10-01 | 0000-00-00 | No | No | Current |
| 0574-0120-08 | 00574012008 | 240 mL in 1 BOTTLE (0574-0120-08) | 240 ml | 1983-10-01 | 2022-01-31 | No | No | Current |
| 0574-0120-74 | 00574012074 | 120 mL in 1 TUBE (0574-0120-74) | 120 ml | 1983-10-01 | 2022-01-31 | No | No | Current |
| 0574-0120-76 | 00574012076 | 240 mL in 1 TUBE (0574-0120-76) | 240 ml | 1983-10-01 | 0000-00-00 | No | No | Current |