Propranolol Hydrochloride
- Product NDC
- 68788-6855
- 11-digit product format
- 687886855
- Labeler code
- 68788
- Product ID
- 68788-6855_5bcb7ddf-fb9a-437c-87e7-459d4d69dc0e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA078494
- Marketing category
- ANDA
- Marketing start
- 2016-12-13
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 60 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 68788-6855-3 | 68788685503 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6855-3) | 2016-12-13 | 0000-00-00 | No | No | Current |