Morphine Sulfate
- Product NDC
- 55700-350
- 11-digit product format
- 557000350
- Labeler code
- 55700
- Product ID
- 55700-350_a04fd3f4-0919-4b6b-ba78-ac9b8c5c029e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Morphine Sulfate
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA202104
- Marketing category
- ANDA
- Marketing start
- 2013-06-30
- Marketing end
- 0000-00-00
- Substance
- MORPHINE SULFATE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-350-60 | 55700035060 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55700-350-60) | 2015-12-23 | 0000-00-00 | No | No | Current |