Lorazepam
- Product NDC
- 67544-870
- 11-digit product format
- 675440870
- Labeler code
- 67544
- Product ID
- 67544-870_dc10ad3e-db44-4346-8945-fe25b0999f9f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lorazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA077657
- Marketing category
- ANDA
- Marketing start
- 2013-03-05
- Marketing end
- 0000-00-00
- Substance
- LORAZEPAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 67544-870-10 | EA - Each | 67544-870 | 3cb77870-d91f-4171-b485-49b3a2ba4e40 | 1 | 2014-05-02 |
| 67544-870-15 | EA - Each | 67544-870 | 57c1fea1-bee0-4c24-b432-2a9f6f11c895 | 1 | 2014-05-02 |
| 67544-870-20 | EA - Each | 67544-870 | 03c7be9f-3ca4-45ab-a41b-b159a5a9fbfb | 1 | 2014-05-02 |
| 67544-870-30 | EA - Each | 67544-870 | b76b4834-8ee7-404f-83be-0c1cb872e170 | 1 | 2014-05-02 |
| 67544-870-45 | EA - Each | 67544-870 | f7136e2a-1644-43d8-8d76-7197e09b8abd | 1 | 2014-05-02 |
| 67544-870-53 | EA - Each | 67544-870 | d686c7f8-0ac8-40a1-82c8-462351de1414 | 1 | 2014-05-02 |
| 67544-870-60 | EA - Each | 67544-870 | a9f0a696-9244-4c3b-aa90-75d807649f8f | 1 | 2014-05-02 |
| 67544-870-70 | EA - Each | 67544-870 | 2dfeeb22-de0c-42b0-bd19-c37008bccb26 | 1 | 2014-05-02 |
| 67544-870-75 | EA - Each | 67544-870 | e0867a42-bb9c-4844-b268-989ad3bac42a | 1 | 2014-05-02 |
| 67544-870-80 | EA - Each | 67544-870 | 40d643dc-c5ff-4847-873c-cc6dd961203b | 1 | 2014-05-02 |
| 67544-870-92 | EA - Each | 67544-870 | 5ff9420f-71be-4ce9-b78b-af19d592b929 | 1 | 2014-05-02 |