NDC 54868-4033
Morphine Sulfate 30 mg tablet, extended release
On the label: Physicians Total Care, Inc.. It's repackaged from NDC 60951-653, made by Par Pharmaceutical (morphine sulfate). That product's FDA listing has since ended, so its label and factories are no longer published.
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 Physicians Total Care, Inc. names for other drugs.
Recalls
- Nov 10, 2010 · Class I · Physicians Total Care, Inc
Labeling: Label mix-up; Bottles labeled to contain Morphine Sulfate IR may contain Morphine Sulfate ER and vice-versa.
Lots: PTC Drug Number: 4033. PTC Batch Number: 65IT. Batch Date: 10/13/2010. Expiration Date: 11/30/2011. NDC: 54868-4033-00
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
- tablet, extended release
- Strength
- 30 mg
- Approval
- ANDA ANDA075295
- On the market since
- Jun 30, 2005
- Package NDCs
54868-4033-054868-4033-154868-4033-254868-4033-354868-4033-454868-4033-5- Official label
- DailyMed (National Library of Medicine), updated Aug 4, 2010
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?