Quick answers
- What is ATROPEN Auto-Injector?
- ATROPEN Auto-Injector is a brand name of Atropine, a prescription medicine. The FDA NDC Directory lists 5 ATROPEN Auto-Injector products in 4 strengths and forms.
- Who makes ATROPEN Auto-Injector?
- MMT holds the FDA application for ATROPEN Auto-Injector (NDA017106, approved May 15, 1973).
- Is there a generic or store brand of ATROPEN Auto-Injector?
- Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a ATROPEN Auto-Injector product. Ask your pharmacist whether one is right for you.
- Has ATROPEN Auto-Injector been recalled?
- No recall linked to ATROPEN Auto-Injector products (by their NDC code or label) appears in the FDA enforcement reports we use.
What ATROPEN Auto-Injector is
Each ATROPEN Auto-Injector product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Atropine · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| atropine 0.25 mg/0.3 mL injection (intramuscular) | ATROPEN Auto-Injector | None listed | DailyMed |
| atropine 0.5 mg/0.7 mL injection (intramuscular) | ATROPEN Auto-Injector | None listed | DailyMed |
| atropine 1 mg/0.7 mL injection (intramuscular) | ATROPEN Auto-Injector | None listed | DailyMed |
| atropine 2 mg/0.7 mL injection (intramuscular) | ATROPEN Auto-Injector | 1 product, 1 company | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Atropine →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA017106 | MMT | May 15, 1973 | 5 |
Companies that list ATROPEN Auto-Injector
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of ATROPEN Auto-Injector products.
- Meridian Medical Technologies LLC5 products
Recalls
No recall linked to ATROPEN Auto-Injector products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.