NDC 67877-242 – Quetiapine
Quetiapine Fumarate 25 mg/1 · Tablet, Film Coated · Oral
Product NDC67877-242
Product details
- Brand name
- Quetiapine
- Generic name
- Quetiapine
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA201504
- Marketed since
- March 1, 2013
- Listing expires
- December 31, 2027
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Quetiapine Fumarate 25 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 67877-242-01 | 100 TABLET, FILM COATED in 1 BOTTLE (67877-242-01) | Mar 1, 2013 |
| 67877-242-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (67877-242-10) | Mar 1, 2013 |
| 67877-242-33 | 1 BLISTER PACK in 1 CARTON (67877-242-33) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Mar 1, 2013 |
| 67877-242-38 | 10 BLISTER PACK in 1 CARTON (67877-242-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Mar 1, 2013 |
Recalls mentioning this NDC
- D-0287-2019 Dec 5, 2018 · Class II
Presence of Foreign Substance; metal shard found in tablet
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- 16729-149 Quetiapine Fumarate 300 mg/1 · Tablet, Film Coated · Accord Healthcare Inc.
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- 67877-245 Quetiapine Fumarate 150 mg/1 · Tablet, Film Coated · Ascend Laboratories, LLC
- 67877-250 Quetiapine Fumarate 100 mg/1 · Tablet, Film Coated · Ascend Laboratories, LLC
- 67877-247 Quetiapine Fumarate 300 mg/1 · Tablet, Film Coated · Ascend Laboratories, LLC
- 67877-246 Quetiapine Fumarate 200 mg/1 · Tablet, Film Coated · Ascend Laboratories, LLC