United States · FDA National Drug Code directory
Pristiq Extended-Release
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0008-1222_b9acfefd-10c0-4942-9446-18bb456efb68
- Product NDC
- 0008-1222
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- desvenlafaxine succinate
- Labeler
- Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20080501
- Source listing expiry
- 20271231
Source-listed ingredients
- DESVENLAFAXINE SUCCINATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0008-1222-01) · 0008-1222-01
- 14 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0008-1222-14) · 0008-1222-14
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0008-1222-30) · 0008-1222-30
- 100 BLISTER PACK in 1 CARTON (0008-1222-50) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 0008-1222-50
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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