DailyMed label
Diphenoxylate Hydrochloride and Atropine Sulfate
DailyMed label · American Health Packaging · version 1
Key facts
| Product | Diphenoxylate Hydrochloride and Atropine Sulfate |
|---|---|
| Labeler | American Health Packaging |
| Document type | HUMAN PRESCRIPTION DRUG LABEL |
| Active ingredients | ATROPINE SULFATE, DIPHENOXYLATE HYDROCHLORIDE |
| Active ingredient UNIIs | 03J5ZE7KA5, W24OD7YW48 |
| Application number | 213335 |
| Route | ORAL |
| DEA schedule | CV |
| NDC package codes | 60687-890-11, 60687-890-01 |
| Effective date | Jul 30, 2025 |
| Set ID | d0a1c80d-6aae-4886-8c25-e2d29ca0836b |
At a glance
- 1–9 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: