DailyMed label
Strattera
DailyMed label · Eli Lilly and Company · version 69
Key facts
| Product | Strattera |
|---|---|
| Labeler | Eli Lilly and Company |
| Document type | HUMAN PRESCRIPTION DRUG LABEL |
| Active ingredients | Atomoxetine hydrochloride |
| Active ingredient UNIIs | 57WVB6I2W0 |
| Application number | 021411 |
| Route | ORAL |
| NDC package codes | 0002-3227-30, 0002-3238-30, 0002-3228-30, 0002-3229-30, 0002-3239-30, 0002-3250-30, 0002-3251-30 |
| Effective date | Jun 30, 2026 |
| Set ID | 309de576-c318-404a-bc15-660c2b1876fb |
At a glance
- 1–9 NDC package codes
- 1–9 Active ingredients
- None Manufacturing establishments listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About DailyMed drug labels
DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.
Source: U.S. National Library of Medicine (NLM), DailyMed · Source date: