Tramadol Hydrochloride 87063-0117
Product NDC
87063-0117- Manufacturer
- Asclemed Usa, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- August 9, 2019
- Listing Expires
- December 31, 2027
- Application
- ANDA211825
Active Ingredients
| Ingredient | Strength |
|---|---|
| Tramadol Hydrochloride | 50 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(8)
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-01)
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-05)
10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-10)
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-20)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-30)
50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-50)
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-60)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-90)