Propranolol Hydrochloride
- Product NDC
- 67296-1380
- 11-digit product format
- 672961380
- Labeler code
- 67296
- Product ID
- 67296-1380_9c9f9369-30b5-3cec-e053-2a95a90a8cef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA078955
- Marketing category
- ANDA
- Marketing start
- 2008-10-13
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-1380-3 | Propranolol Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1380 | PROPRANOLOL HYDROCHLORIDE TABLET [REDPHARM DRUG, INC.] | 2 | Legacy NDC, 1 package rows | 20200121_504c0f1c-b0cd-4aae-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-1380-3 | 67296138003 | 30 TABLET in 1 BOTTLE (67296-1380-3) | 30 tablet | 2008-10-13 | 0000-00-00 | No | No | Current |