Bupropion Hydrochloride
- Product NDC
- 63629-6438
- 11-digit product format
- 636296438
- Labeler code
- 63629
- Product ID
- 63629-6438_1ce875b8-1c8f-4537-84c7-e636a1a65f0b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA079095
- Marketing category
- ANDA
- Marketing start
- 2009-07-02
- Marketing end
- 0000-00-00
- Substance
- BUPROPION HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6438-1 | 63629643801 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-6438-1) | 2015-09-17 | 0000-00-00 | No | No | Current |
| 63629-6438-2 | 63629643802 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-6438-2) | 2017-02-21 | 0000-00-00 | No | No | Current |