Bupropion hydrochloride 150 mg / 1 Tablet 500 Tablet, Film Coated, Extended Release
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 69097-0071-12 |
|---|---|
| Product NDC | 69097-0071 |
| Generic Drug Name | Bupropion hydrochloride |
| Brand Name | Bupropion Hydrochloride |
| Manufacturer | Cipla USA., Inc. |
| Strength | 150 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 500 Tablet, Film Coated, Extended Release |
| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-071-12) |
| Active Ingredients | Bupropion Hydrochloride |
| Marketing Category | ANDA |
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NDC snapshot
Bupropion hydrochloride 150 mg / 1 Tablet is tracked under NDC 69097-0071-12 and rolls up into product family 69097-0071. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.
- Package configuration: 500 Tablet, Film Coated, Extended Release.
- Manufacturer: Cipla USA., Inc..
- Dosage form: Tablet.
- Family size: 1 indexed presentation.
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Official references
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Potential alternatives with matching presentation
Open the comparison hub or review package-level listings from 5 product-NDC families with matching normalized presentation details. Review each product detail page before treating any item as a true alternative.
Bupropion hydrochloride 150 mg / 1 Tablet 500 Tablet, Film Coated, Extended Release, NDC 69097-0071-12, is a Cipla USA., Inc. 150 mg / 1 tablet presentation packaged as 500 Tablet, Film Coated, Extended Release.
NDC search formats
- Canonical NDC 11: 69097-0071-12
- Digits-only NDC 11: 69097007112
- Possible 10-digit display format: 69097-071-12 (6909707112)
Helpful product links
- Search by brand name: Bupropion Hydrochloride
- NDC 11: 69097-0071-12
- Product family NDC: 69097-0071
- VA classification code: CN609
- VA classification code description: ANTIDEPRESSANTS,OTHER
- CMOP ID: B0585
- VUID: 4026567