Morphine Sulfate
- Product NDC
- 67296-1561
- 11-digit product format
- 672961561
- Labeler code
- 67296
- Product ID
- 67296-1561_d61bf800-8542-75ea-e053-2a95a90aca60
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Morphine Sulfate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA074862
- Marketing category
- ANDA
- Marketing start
- 2011-01-14
- Marketing end
- 0000-00-00
- Substance
- MORPHINE SULFATE
- Active strength
- 15 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA], Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-1561-2 | Morphine Sulfate | 20 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 20 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1561 | MORPHINE SULFATE TABLET, FILM COATED, EXTENDED RELEASE [REDPHARM DRUG, INC.] | 5 | Legacy NDC, 1 package rows | 20220122_5bfee7cd-a242-3119-e053-2991aa0ab355.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-1561-2 | 67296156102 | 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67296-1561-2) | 2011-01-14 | 0000-00-00 | No | No | Current |