Propranolol Hydrochloride
- Product NDC
- 60687-306
- 11-digit product format
- 606870306
- Labeler code
- 60687
- Product ID
- 60687-306_d61b80b1-42b7-c057-e053-2a95a90a8558
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA070176
- Marketing category
- ANDA
- Marketing start
- 2017-07-15
- Marketing end
- 2022-09-30
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 20 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-306-01 | 60687030601 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-306-01) > 1 TABLET in 1 BLISTER PACK (60687-306-11) | 100 blister pack | 2017-07-15 | 0000-00-00 | No | No | Current |