Propafenone Hydrochloride
- Product NDC
- 60687-185
- 11-digit product format
- 606870185
- Labeler code
- 60687
- Product ID
- 60687-185_ea3f6631-a727-1904-e053-2995a90aa4d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propafenone hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA078540
- Marketing category
- ANDA
- Marketing start
- 2016-01-29
- Marketing end
- 2024-09-30
- Substance
- PROPAFENONE HYDROCHLORIDE
- Active strength
- 225 mg/1
- Pharmacologic classes
- Antiarrhythmic [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 |
|---|
| 60687-185-32 | 60687018532 | 20 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-185-32) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (60687-185-33) | 20 blister pack | 2016-01-29 | 0000-00-00 | No | No | Current |