Tramadol Hydrochloride
- Product NDC
- 35356-659
- 11-digit product format
- 353560659
- Labeler code
- 35356
- Product ID
- 35356-659_1c1ab81f-0f11-4d10-8986-4e1a1b779bd9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tramadol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA076003
- Marketing category
- ANDA
- Marketing start
- 2009-11-23
- Marketing end
- 0000-00-00
- Substance
- TRAMADOL HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 35356-659-01 | EA - Each | 35356-659 | ea00e1cb-e405-41f4-bb29-610a10fdb882 | 1 | 2013-02-13 |
| 35356-659-08 | EA - Each | 35356-659 | 843144a3-6b8b-462b-b3f8-b5b606b9701b | 1 | 2014-05-02 |
| 35356-659-12 | EA - Each | 35356-659 | ad54f580-e21c-4824-993c-ae36110c3521 | 1 | 2016-12-07 |
| 35356-659-15 | EA - Each | 35356-659 | 45b9eb20-9855-458c-8a11-88b4e17c7ac0 | 1 | 2014-05-02 |
| 35356-659-18 | EA - Each | 35356-659 | e413b7cf-f0ff-407f-ab69-684e6d03a642 | 1 | 2013-02-13 |
| 35356-659-20 | EA - Each | 35356-659 | 74984907-f961-496c-b8dd-0bd1532e803c | 1 | 2013-02-13 |
| 35356-659-24 | EA - Each | 35356-659 | 1c3278cc-329c-40d2-b6d6-4e88b9706621 | 1 | 2013-02-13 |
| 35356-659-30 | EA - Each | 35356-659 | 335e694f-a3dd-49e9-9c4f-1cadcabca0df | 1 | 2013-02-13 |
| 35356-659-40 | EA - Each | 35356-659 | 4aa862a3-af8a-482a-8544-fd9bc8f753a7 | 1 | 2013-07-02 |
| 35356-659-60 | EA - Each | 35356-659 | 2baedb8c-da4d-4e2f-b678-db3802060268 | 1 | 2013-02-13 |
| 35356-659-90 | EA - Each | 35356-659 | c6f9e25f-be99-412e-ac6f-33982965be4c | 1 | 2013-02-13 |