Bupropion Hydrochloride
- Product NDC
- 55154-7986
- 11-digit product format
- 551547986
- Labeler code
- 55154
- Product ID
- 55154-7986_867a28c5-dcad-4614-971b-4c72034b83be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA075932
- Marketing category
- ANDA
- Marketing start
- 2004-03-22
- Marketing end
- 0000-00-00
- Substance
- BUPROPION HYDROCHLORIDE
- Active strength
- 150 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
- 2023-12-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-7986-0 | 55154798600 | 10 BLISTER PACK in 1 BAG (55154-7986-0) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 10 blister pack | 2004-03-22 | 0000-00-00 | No | No | Current |