Prednisone
- Product NDC
- 55700-209
- 11-digit product format
- 557000209
- Labeler code
- 55700
- Product ID
- 55700-209_89e74a02-2bb0-4307-bfc1-ada13e640939
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA040362
- Marketing category
- ANDA
- Marketing start
- 2001-08-29
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55700-209 | PREDNISONE (PREDNISONE) TABLET [QUALITY CARE PRODUCTS LLC] | 15 | Legacy NDC | 20241218_4cc5a365-b50c-4ce2-a16b-f9467bb5896b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-209-15 | 55700020915 | 15 TABLET in 1 BOTTLE (55700-209-15) | 15 tablet | 2015-09-04 | 0000-00-00 | No | No | Current |
| 55700-209-21 | 55700020921 | 21 TABLET in 1 BOTTLE (55700-209-21) | 21 tablet | 2015-01-16 | 0000-00-00 | No | No | Current |
| 55700-209-30 | 55700020930 | 30 TABLET in 1 BOTTLE (55700-209-30) | 30 tablet | 2015-01-16 | 0000-00-00 | No | No | Current |
| 55700-209-42 | 55700020942 | 42 TABLET in 1 BOTTLE (55700-209-42) | 42 tablet | 2015-01-16 | 0000-00-00 | No | No | Current |
| 55700-209-48 | 55700020948 | 48 TABLET in 1 BOTTLE (55700-209-48) | 48 tablet | 2017-08-11 | 0000-00-00 | No | No | Current |