Actidose Aqua
- Product NDC
- 0574-0121
- 11-digit product format
- 005740121
- Labeler code
- 0574
- Product ID
- 0574-0121_48354f4f-3b95-4da4-b60d-ac97618fae04
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- activated charcoal
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Padagis US LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1984-01-01
- Marketing end
- 2022-12-31
- 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
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 |
|---|
| 0574-0121-04 | 00574012104 | 120 mL in 1 BOTTLE (0574-0121-04) | 120 ml | 1984-01-01 | 2022-01-31 | No | No | Current |
| 0574-0121-08 | 00574012108 | 240 mL in 1 BOTTLE (0574-0121-08) | 240 ml | 1984-01-01 | 0000-00-00 | No | No | Current |
| 0574-0121-25 | 00574012125 | 72 mL in 1 TUBE (0574-0121-25) | 72 ml | 1984-01-01 | 2022-12-31 | No | No | Current |
| 0574-0121-74 | 00574012174 | 120 mL in 1 TUBE (0574-0121-74) | 120 ml | 1984-01-01 | 2021-12-31 | No | No | Current |
| 0574-0121-76 | 00574012176 | 240 mL in 1 TUBE (0574-0121-76) | 240 ml | 1984-01-01 | 2022-01-31 | No | No | Current |