TRAMADOL HYDROCHLORIDE
- Product NDC
- 68788-6929
- 11-digit product format
- 687886929
- Labeler code
- 68788
- Product ID
- 68788-6929_030e59df-588f-43ce-8a35-7488a3f0526d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TRAMADOL HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA090404
- Marketing category
- ANDA
- Marketing start
- 2017-03-22
- Marketing end
- 0000-00-00
- Substance
- TRAMADOL HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 68788-6929-1 | EA - Each | 68788-6929 | d4641bdf-9fe7-47b7-8e19-f20c0e80ec71 | 1 | 2019-08-06 |
| 68788-6929-2 | EA - Each | 68788-6929 | ad780bff-4518-4ee7-831f-954bfd455d82 | 1 | 2019-08-06 |
| 68788-6929-3 | EA - Each | 68788-6929 | b64a2ad1-3ded-4191-a426-97396932369f | 1 | 2019-08-06 |
| 68788-6929-4 | EA - Each | 68788-6929 | f6b14c5e-6342-4f19-bdbe-e6f792167a0e | 1 | 2019-08-06 |
| 68788-6929-5 | EA - Each | 68788-6929 | 2f60aa77-e3c7-4442-a0cd-e338c8c5cd79 | 1 | 2019-08-06 |
| 68788-6929-6 | EA - Each | 68788-6929 | df24a8d0-0e24-4223-8d9a-84d809fa5ca4 | 1 | 2019-08-06 |
| 68788-6929-7 | EA - Each | 68788-6929 | 24ba86d7-00d9-4cf1-a6dd-e6469d24adfd | 1 | 2019-08-06 |
| 68788-6929-8 | EA - Each | 68788-6929 | fc50a2d5-5441-45fa-8b7b-810dfbd5ecc1 | 1 | 2019-08-06 |
| 68788-6929-9 | EA - Each | 68788-6929 | 478799e9-bbe5-46bb-8d88-f38eba69a5d4 | 1 | 2019-08-06 |