NDCFind

Tramadol Hydrochloride 71205-0708-90

Package NDC

71205-0708-90

Product NDC: 71205-0708

Manufacturer
Proficient Rx Lp
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIV
Marketing Start
December 12, 2011
Listing Expires
December 31, 2026
Application
ANDA201384

Active Ingredients

IngredientStrength
Tramadol Hydrochloride200 mg/1

Drug Class

Full Opioid Agonists [MoA]Opioid Agonist [EPC]

Selected Package

71205-0708-90Selected

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-90)

Other packages for this product(2)

71205-0708-30

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-30)

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71205-0708-60

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-60)

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Related Products

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External Resources

FDA Drug DatabaseDailyMed Label