NDC 0069-1345 - Paxlovid
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 0069-1345
- Package NDCs from labels
- 0069-1345-11, 0069-1345-05, 0069-1345-01
- Manufacturer
- Pfizer Laboratories Div Pfizer Inc | Pfizer Inc | Pfizer Ireland Pharmaceuticals Unlimited Company | Pfizer Manufacturing Deutschland GmbH | Pfizer Italia S.r.l. | Pharmacia & Upjohn Company LLC
- Effective date
- 2026-02-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Paxlovid | Pfizer Laboratories Div Pfizer Inc | Pfizer Inc | Pfizer Ireland Pharmaceuticals Unlimited Company | Pfizer Manufacturing Deutschland GmbH | Pfizer Italia S.r.l. | Pharmacia & Upjohn Company LLC | 2026-02-19 | HUMAN PRESCRIPTION DRUG LABEL |
| Paxlovid | Pfizer Laboratories Div Pfizer Inc | Pfizer Inc | AbbVie Deutschland GmbH & Co KG | AbbVie SRL | Pfizer Ireland Pharmaceuticals | Pfizer Manufacturing Deutschland GmbH | AndersonBrecon Inc. | Changzhou SynTheAll Pharmaceutical Co., Ltd | Jilin Asymchem Laboratories Co., Ltd. | Sharp Packaging Services, LLC | Hetero Drugs Limited | Hetero Labs Limited | Pfizer Italia S.r.l. | Esteve Quimica, S.A. | Patheon Inc. | Pharmaprogress SRL | 2023-11-07 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0069-1345-05 | Paxlovid | 5 in 1 BLISTER PACK | TABLET, FILM COATED | 5 | 100 mg | 12 |
| 0069-1345-11 | Paxlovid | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | 100 mg | 12 |
| 0069-1345-11 | Paxlovid | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | 100 mg | 12 |
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.