BUPROPION HYDROCHLORIDE
- Product NDC
- 69844-011
- 11-digit product format
- 698440011
- Labeler code
- 69844
- Product ID
- 69844-011_914eea2c-eb30-42ac-a437-41bfb3207e11
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BUPROPION HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Graviti Pharmaceuticals Private Limited
- Application
- ANDA211020
- Marketing category
- ANDA
- Marketing start
- 2019-01-28
- 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 |
|---|
| 69844-011-01 | 69844001101 | 30 TABLET in 1 BOTTLE (69844-011-01) | 30 tablet | 2019-01-28 | 0000-00-00 | No | No | Current |
| 69844-011-02 | 69844001102 | 90 TABLET in 1 BOTTLE (69844-011-02) | 90 tablet | 2019-01-28 | 0000-00-00 | No | No | Current |
| 69844-011-03 | 69844001103 | 1000 TABLET in 1 BOTTLE (69844-011-03) | 1000 tablet | 2019-01-28 | 0000-00-00 | No | No | Current |