NDC 0555-9009 – Nortrel 21 Day
Norethindrone 1 mg/1; Ethinyl Estradiol .035 mg/1 · Tablet · Oral
Product NDC0555-9009
Product details
- Brand name
- Nortrel 21 Day
- Generic name
- Norethindrone and Ethinyl Estradiol
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA072693
- Marketed since
- June 13, 2001
- Listing expires
- December 31, 2027
- Pharmacologic class
- Estrogen; Progestin
Active ingredients
- Norethindrone 1 mg/1
- Ethinyl Estradiol .035 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0555-9009-42 | 3 POUCH in 1 CARTON (0555-9009-42) / 1 BLISTER PACK in 1 POUCH (0555-9009-80) / 21 TABLET in 1 BLISTER PACK | Jun 13, 2001 |
Recalls mentioning this NDC
- D-0321-2024 Feb 21, 2024 · Class III
Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets.
Other Nortrel products
- 50090-3229 · Kit · A-S Medication Solutions
- 0555-9008 · Kit · Teva Pharmaceuticals USA, Inc.
- 0555-9010 · Kit · Teva Pharmaceuticals USA, Inc.