NDC 68000-110
Morphine Sulfate 20 mg per 1 mL solution
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Cranbury Pharmaceuticals, LLC's NDC 27808-082.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Cranbury Pharmaceuticals, LLC names for other drugs.
Recalls
- Jun 15, 2017 · Class II · Tris Pharma Inc.
Defective container: Oral solution leaking from container.
Lots: Lot #: 08215001A, Exp 6/30/2017; 08215002A, 08215004A, Exp 7/31/2017
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Morphine: every company that makes it
- Form
- solution, oral
- Strength
- 20 mg per 1 mL
- Approval
- ANDA ANDA203518
- On the market since
- May 1, 2026
- Package NDCs
68000-110-0168000-110-06- Official label
- DailyMed (National Library of Medicine), updated May 1, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?