NDC 59011-440 – OxyContin
Oxycodone Hydrochloride 40 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC59011-440
Product details
- Brand name
- OxyContin
- Generic name
- Oxycodone hydrochloride
- Labeler
- Knoa Pharma LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- NDA · NDA022272
- Marketed since
- August 8, 2010
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Oxycodone Hydrochloride 40 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 59011-440-10 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011-440-10) | Aug 8, 2010 |
| 59011-440-20 | 2 BLISTER PACK in 1 CARTON (59011-440-20) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Aug 8, 2010 |
Other OxyContin products
- 59011-410 Oxycodone Hydrochloride 10 mg/1 · Tablet, Film Coated, Extended Release · Knoa Pharma LLC
- 59011-415 Oxycodone Hydrochloride 15 mg/1 · Tablet, Film Coated, Extended Release · Knoa Pharma LLC
- 59011-420 Oxycodone Hydrochloride 20 mg/1 · Tablet, Film Coated, Extended Release · Knoa Pharma LLC
- 59011-430 Oxycodone Hydrochloride 30 mg/1 · Tablet, Film Coated, Extended Release · Knoa Pharma LLC
- 59011-460 Oxycodone Hydrochloride 60 mg/1 · Tablet, Film Coated, Extended Release · Knoa Pharma LLC
- 59011-480 Oxycodone Hydrochloride 80 mg/1 · Tablet, Film Coated, Extended Release · Knoa Pharma LLC