DailyMed label
Venlafaxine hydrochloride
DailyMed label · Dr. Reddy's Laboratories Limited · version 13
Key facts
| Product | Venlafaxine hydrochloride |
|---|---|
| Labeler | Dr. Reddy's Laboratories Limited |
| Document type | HUMAN PRESCRIPTION DRUG LABEL |
| Active ingredients | Venlafaxine hydrochloride |
| Active ingredient UNIIs | 7D7RX5A8MO |
| Application number | 078301 |
| Route | ORAL |
| NDC package codes | 55111-545-30, 55111-545-60, 55111-545-90, 55111-545-01, 55111-545-05, 55111-545-79, 55111-546-30, 55111-546-60, 55111-546-90, 55111-546-01, 55111-546-05, 55111-546-79 and 18 more |
| Effective date | Dec 23, 2022 |
| Set ID | 106d0d7b-925b-74e7-83cb-562144ce1f92 |
At a glance
- 10–99 NDC package codes
- 1–9 Active ingredients
- 1–9 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: