PRAVASTATIN SODIUM
- Product NDC
- 72162-1953
- 11-digit product format
- 721621953
- Labeler code
- 72162
- Product ID
- 72162-1953_72d78298-266a-45d6-9577-b4f3737134ab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA209869
- Marketing category
- ANDA
- Marketing start
- 2021-02-01
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 40 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- PRAVASTATIN SODIUM
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PRAVASTATIN SODIUM | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3M8608UQ61 |
| Rxcui | 904475 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1953-0 | PRAVASTATIN SODIUM | 1000 in 1 BOTTLE | TABLET | 1000 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1953 | PRAVASTATIN SODIUM TABLET [BRYANT RANCH PREPACK] | 101 | Current NDC, 1 package rows | 20250521_51800012-406b-4389-817f-88dd21e338d1.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1953-0 | 72162195300 | 1000 TABLET in 1 BOTTLE (72162-1953-0) | 1000 tablet | 2024-03-11 | No | No | Historical |