Prednisone
- Product NDC
- 0143-9740
- 11-digit product format
- 001439740
- Labeler code
- 0143
- Product ID
- 0143-9740_92e5952b-2b1e-42c7-a8b3-c33d403d47aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- West-ward Pharmaceuticals Corp
- Application
- ANDA080292
- Marketing category
- ANDA
- Marketing start
- 2009-08-03
- Marketing end
- 2022-06-30
- Substance
- PREDNISONE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 2205d503-be51-445b-bb34-c209cc557b3c | Product name | 5 | 20230105 |
| 9492a99d-61c8-491f-9086-1c6a7e98c040 | Product name | 6 | 20230105 |
| 205c2cdd-a63b-cbc9-6bcb-6be6001edf81 | Product name | 2 | 20170705 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0143-9740-01 | EA - Each | 0143-9740 | 260a4555-2df7-4ce2-8396-00dc3dfc956e | 1 | 2013-04-01 |
| 0143-9740-10 | EA - Each | 0143-9740 | ee33d7e2-a362-4c5e-9f65-7e455229b1dd | 1 | 2013-04-01 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| PREDNISONE | ACTIVE INGREDIENT | VB0R961HZT | PREDNISONE TABLET PREDNISONE TABLET [DIRECT RX] | 1 | |
| PREDNISONE | ACTIVE MOIETY | VB0R961HZT | PREDNISONE TABLET PREDNISONE TABLET [DIRECT RX] | 1 | |
| ANHYDROUS LACTOSE | INACTIVE INGREDIENT | 3SY5LH9PMK | PREDNISONE TABLET PREDNISONE TABLET [DIRECT RX] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | PREDNISONE TABLET PREDNISONE TABLET [DIRECT RX] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | PREDNISONE TABLET PREDNISONE TABLET [DIRECT RX] | 1 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | PREDNISONE TABLET PREDNISONE TABLET [DIRECT RX] | 1 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | PREDNISONE TABLET PREDNISONE TABLET [DIRECT RX] | 1 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | PREDNISONE TABLET PREDNISONE TABLET [DIRECT RX] | 1 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 198145 | predniSONE 10 MG Oral Tablet | PSN | a10ce97b-3efc-443f-9c76-a2bfe2c57be3 | 3 |
| 312617 | predniSONE 5 MG Oral Tablet | PSN | a10ce97b-3efc-443f-9c76-a2bfe2c57be3 | 3 |
| 198145 | prednisone 10 MG Oral Tablet | SCD | a10ce97b-3efc-443f-9c76-a2bfe2c57be3 | 3 |
| 312617 | prednisone 5 MG Oral Tablet | SCD | a10ce97b-3efc-443f-9c76-a2bfe2c57be3 | 3 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0143-9740-10 | 00143974010 | 1000 TABLET in 1 BOTTLE (0143-9740-10) | 1000 tablet | 2009-08-03 | 2022-06-30 | No | No | Current |