Bupropion hydrochloride
- Product NDC
- 64725-0736
- 11-digit product format
- 647250736
- Labeler code
- 64725
- Product ID
- 64725-0736_a48f17ec-bca5-486d-a68e-aceaa66d57c6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- TYA Pharmaceuticals
- Application
- ANDA078866
- Marketing category
- ANDA
- Marketing start
- 2010-04-08
- 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
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 64725-0736-1 | Bupropion hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 100 | | 4 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| BUPROPION HYDROCHLORIDE | ACTIVE INGREDIENT | ZG7E5POY8O | BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 4 | |
| BUPROPION | ACTIVE MOIETY | 01ZG3TPX31 | BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 4 | |
| ANHYDROUS LACTOSE | INACTIVE INGREDIENT | 3SY5LH9PMK | BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 4 | |
| HYDROXYPROPYL CELLULOSE (TYPE H) | INACTIVE INGREDIENT | RFW2ET671P | BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 4 | |
| POLYETHYLENE GLYCOL 3350 | INACTIVE INGREDIENT | G2M7P15E5P | BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 4 | |
| POLYVINYL ALCOHOL | INACTIVE INGREDIENT | 532B59J990 | BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 4 | |
| SACCHARIN | INACTIVE INGREDIENT | FST467XS7D | BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 4 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 4 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 4 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 4 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 4 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64725-0736 | BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 4 | Legacy NDC, 1 package rows | 20140901_6d6ec7d4-e3f4-4ade-b76b-49a9bb6d61c5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64725-0736-1 | 64725073601 | 100 in 1 BOTTLE | Historical |