NDC 0603-5338 – Prednisone
Prednisone 10 mg/1 · Tablet · Oral
Product NDC0603-5338
Product details
- Brand name
- Prednisone
- Generic name
- Prednisone
- Labeler
- Par Health USA, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA040256
- Marketed since
- July 12, 2002
- Listing expires
- December 31, 2027
- Pharmacologic class
- Corticosteroid
Active ingredients
- Prednisone 10 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 0603-5338-15 | 21 TABLET in 1 BOX, UNIT-DOSE (0603-5338-15) | Jul 12, 2002 |
| 0603-5338-21 | 100 TABLET in 1 BOTTLE, PLASTIC (0603-5338-21) | Jul 12, 2002 |
| 0603-5338-28 | 500 TABLET in 1 BOTTLE, PLASTIC (0603-5338-28) | Jul 12, 2002 |
| 0603-5338-31 | 48 TABLET in 1 BOX, UNIT-DOSE (0603-5338-31) | Jul 12, 2002 |
| 0603-5338-32 | 1000 TABLET in 1 BOTTLE, PLASTIC (0603-5338-32) | Jul 12, 2002 |
Recalls mentioning this NDC
- D-1035-2020 Mar 25, 2020 · Class III
Labeling: Incorrect or Missing Exp Date - An incorrect expiration date has been identified on Prednisone Tablets USP 5 mg
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