Prednisone
- Product NDC
- 55700-728
- 11-digit product format
- 557000728
- Labeler code
- 55700
- Product ID
- 55700-728_5d111514-ec45-4b8c-83ec-d2c7b441e1c0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA085161
- Marketing category
- ANDA
- Marketing start
- 2019-03-01
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 55700-728-20 | 2025-01-10 | C162847 | 48780-1 | ba0f9c33-3624-a910-e053-dadaa90a0b85 | b0826cf5-33ac-4e24-93d7-caf6bee2b969 |
| 55700-728-21 | 2025-01-10 | C162847 | 48780-1 | ba0f9c33-3624-a910-e053-dadaa90a0b85 | b0826cf5-33ac-4e24-93d7-caf6bee2b969 |
| 55700-728-20 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-3624-a910-e053-dadaa90a0b85 | b0826cf5-33ac-4e24-93d7-caf6bee2b969 |
| 55700-728-21 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-3624-a910-e053-dadaa90a0b85 | b0826cf5-33ac-4e24-93d7-caf6bee2b969 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 55700-728-20 | EA - Each | 55700-728 | c50e8146-be16-4aa6-bf32-b676056fc7e3 | 1 | 2019-06-19 |
| 55700-728-21 | EA - Each | 55700-728 | 28c8aaab-3616-41d1-8eb4-ca141527c909 | 1 | 2019-04-11 |