Bupropion Hydrochloride
- Product NDC
- 67046-077
- 11-digit product format
- 670460077
- Labeler code
- 67046
- Product ID
- 67046-077_59783eee-adc6-3327-e053-2991aa0ab6f5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- ANDA076143
- Marketing category
- ANDA
- Marketing start
- 2006-01-17
- Marketing end
- 0000-00-00
- Substance
- BUPROPION HYDROCHLORIDE
- Active strength
- 75 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67046-077-30 | Bupropion Hydrochloride | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67046-077 | BUPROPION HYDROCHLORIDE TABLET, FILM COATED [CONTRACT PHARMACY SERVICES-PA] | 1 | Legacy NDC, 1 package rows | 20170918_59783eee-adc5-3327-e053-2991aa0ab6f5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 67046-077-30 | 67046007730 | 30 in 1 BLISTER PACK | Historical |