Pravastatin Sodium
- Product NDC
- 63629-3563
- 11-digit product format
- 636293563
- Labeler code
- 63629
- Product ID
- 63629-3563_54fae935-fb40-4def-b552-1e34d6437e77
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076939
- Marketing category
- ANDA
- Marketing start
- 2006-10-23
- Marketing end
- 0000-00-00
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 20 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63629-3563-1 | 2021-07-01 | C162847 | 48780-1 | 9855e2a2-4053-60a7-e053-dbdaa90a05bd | d528962f-cebd-4425-8ed5-843866683eca |
| 63629-3563-2 | 2021-07-01 | C162847 | 48780-1 | 9855e2a2-4053-60a7-e053-dbdaa90a05bd | d528962f-cebd-4425-8ed5-843866683eca |
| 63629-3563-3 | 2021-07-01 | C162847 | 48780-1 | 9855e2a2-4053-60a7-e053-dbdaa90a05bd | d528962f-cebd-4425-8ed5-843866683eca |
| 63629-3563-1 | 2019-11-27 | C162847 | 48780-1 | 9855e2a2-4053-60a7-e053-dbdaa90a05bd | d528962f-cebd-4425-8ed5-843866683eca |
| 63629-3563-2 | 2019-11-27 | C162847 | 48780-1 | 9855e2a2-4053-60a7-e053-dbdaa90a05bd | d528962f-cebd-4425-8ed5-843866683eca |
| 63629-3563-3 | 2019-11-27 | C162847 | 48780-1 | 9855e2a2-4053-60a7-e053-dbdaa90a05bd | d528962f-cebd-4425-8ed5-843866683eca |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63629-3563-1 | EA - Each | 63629-3563 | fece4c07-957e-483a-83c9-f63a28ddefe4 | 1 | 2013-02-13 |