Propafenone Hydrochloride
- Product NDC
- 60687-537
- 11-digit product format
- 606870537
- Labeler code
- 60687
- Product ID
- 60687-537_e271f15f-9dfd-8e72-e053-2a95a90ab2a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propafenone Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA075938
- Marketing category
- ANDA
- Marketing start
- 2020-06-01
- Marketing end
- 2023-02-28
- Substance
- PROPAFENONE HYDROCHLORIDE
- Active strength
- 150 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 |
|---|
| 60687-537-01 | 60687053701 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-537-01) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-537-11) | 100 blister pack | 2020-06-01 | 0000-00-00 | No | No | Current |