Propranolol Hydrochloride
- Product NDC
- 71335-0907
- 11-digit product format
- 713350907
- Labeler code
- 71335
- Product ID
- 71335-0907_46438296-1f61-4b5d-9be2-3dcf6b37bb99
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propranolol hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA018553
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2017-12-21
- Marketing end
- 2023-05-31
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 120 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0907-1 | 71335090701 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0907-1) | 2018-07-18 | 2023-05-31 | No | No | Current |
| 71335-0907-2 | 71335090702 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0907-2) | 2018-07-18 | 2023-05-31 | No | No | Current |
| 71335-0907-3 | 71335090703 | 180 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0907-3) | 2018-07-18 | 2023-05-31 | No | No | Current |
| 71335-0907-4 | 71335090704 | 18 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0907-4) | 2018-07-18 | 2023-05-31 | No | No | Current |
| 71335-0907-5 | 71335090705 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0907-5) | 2018-07-18 | 2023-05-31 | No | No | Current |