Propranolol Hydrochloride
- Product NDC
- 60429-129
- 11-digit product format
- 604290129
- Labeler code
- 60429
- Product ID
- 60429-129_c137d572-6f4d-2fcd-e053-2995a90a8e56
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA078494
- Marketing category
- ANDA
- Marketing start
- 2014-07-15
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 160 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 60429-129-01 | 60429012901 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (60429-129-01) | 2014-07-15 | 0000-00-00 | No | No | Current |
| 60429-129-05 | 60429012905 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (60429-129-05) | 2014-07-15 | 0000-00-00 | No | No | Current |