Propranolol Hydrochloride
- Product NDC
- 21695-668
- 11-digit product format
- 216950668
- Labeler code
- 21695
- Product ID
- 21695-668_9ab4058c-86fa-41c8-8291-e073fd28257f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA070176
- Marketing category
- ANDA
- Marketing start
- 1986-01-01
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 21695-668-60 | Propranolol Hydrochloride | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
| 21695-668-78 | Propranolol Hydrochloride | 180 in 1 BOTTLE | TABLET | 180 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-668 | PROPRANOLOL HYDROCHLORIDE TABLET [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 2 package rows | 20101201_9ab4058c-86fa-41c8-8291-e073fd28257f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-668-60 | 21695066860 | 60 in 1 BOTTLE | Historical |
| 21695-668-78 | 21695066878 | 180 in 1 BOTTLE | Historical |