Tramadol Hydrochloride
- Product NDC
- 76420-733
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tramadol Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA208708
- Marketing category
- ANDA
- Substance
- TRAMADOL HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 76420-733-00 | 1000 TABLET, COATED in 1 BOTTLE (76420-733-00) | 2024-05-22 | | No | Historical |
| 76420-733-01 | 100 TABLET, COATED in 1 BOTTLE (76420-733-01) | 2024-05-22 | | No | Historical |
| 76420-733-02 | 2 TABLET, COATED in 1 BOTTLE (76420-733-02) | 2025-08-14 | | No | Historical |
| 76420-733-05 | 500 TABLET, COATED in 1 BOTTLE (76420-733-05) | 2024-05-22 | | No | Historical |
| 76420-733-10 | 1 TABLET, COATED in 1 BOTTLE (76420-733-10) | 2025-08-14 | | No | Historical |
| 76420-733-12 | 120 TABLET, COATED in 1 BOTTLE (76420-733-12) | 2025-07-14 | | No | Historical |
| 76420-733-30 | 30 TABLET, COATED in 1 BOTTLE (76420-733-30) | 2024-05-22 | | No | Historical |
| 76420-733-60 | 60 TABLET, COATED in 1 BOTTLE (76420-733-60) | 2024-05-22 | | No | Historical |
| 76420-733-90 | 90 TABLET, COATED in 1 BOTTLE (76420-733-90) | 2024-05-22 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Tramadol Hydrochloride | Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | 2025-08-14 | HUMAN PRESCRIPTION DRUG LABEL | 3 |