Chloramphenicol
- Manufacturer
- AMERICAN PHARMACEUTICAL INGREDIENTS LLC
- Effective date
- 2013-11-01
- Label type
- BULK INGREDIENT
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:47:50
Label at a glance#
ProductChloramphenicol
Active ingredientCHLORAMPHENICOL
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 58597-7007-4 | Chloramphenicol | 25000 g in 1 CONTAINER | POWDER | 25000 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 58597-7007 | CHLORAMPHENICOL POWDER [AMERICAN PHARMACEUTICAL INGREDIENTS LLC] | 1 | 1 package rows | 20131101_ff489ec6-e0dc-4b32-b519-ad2e21f36e42.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| CHLORAMPHENICOL | ACTIVE INGREDIENT | 66974FR9Q1 | 1 | |
| CHLORAMPHENICOL | ACTIVE MOIETY | 66974FR9Q1 | 1 |
Products#
Every source-derived product name is available through these pages.
- Chloramphenicol
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 58597-7007 | 58597-7007-4 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CHLORAMPHENICOL | 66974FR9Q1 | ACTIB |
Source Document#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
