Drug
Tiagabine Hydrochloride NDC Codes
Tiagabine Hydrochloride is listed in the FDA NDC Directory as 10 finished products from 3 labelers.
Overview
Active ingredient: Tiagabine hydrochloride. Each product below links to its own NDC page with package NDCs in 10- and 11-digit form.
- Generic name
- Tiagabine Hydrochloride
- Active ingredients
- Tiagabine hydrochloride
- Labelers
- Novadoz Pharmaceuticals LLC, Teva Pharmaceuticals USA, Inc., Sun Pharmaceutical Industries, Inc.
- Strengths
- Tiagabine hydrochloride 2 mg/1; Tiagabine hydrochloride 4 mg/1; Tiagabine hydrochloride 12 mg/1; Tiagabine hydrochloride 16 mg/1
- Dosage forms
- Tablet, Film coated, Tablet
- Routes
- Oral
- Drug classes (FDA established)
- Anti-epileptic Agent
- HCPCS / J-code
- None in Med-Code's directory for these products
- Package NDCs
- 14
NDC codes
Newest listings first. Each row links to the product’s NDC page.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) | HCPCS |
|---|---|---|---|---|---|---|
| Tiagabine Hydrochloride | Tiagabine hydrochloride 2 mg/1 | TabletOral | Novadoz Pharmaceuticals LLC | 72205-084 | 72205-0084-30 | — |
| Tiagabine Hydrochloride | Tiagabine hydrochloride 4 mg/1 | TabletOral | Novadoz Pharmaceuticals LLC | 72205-085 | 72205-0085-30 | — |
| Tiagabine Hydrochloride | Tiagabine hydrochloride 12 mg/1 | TabletOral | Novadoz Pharmaceuticals LLC | 72205-086 | 72205-0086-30 | — |
| Tiagabine Hydrochloride | Tiagabine hydrochloride 16 mg/1 | TabletOral | Novadoz Pharmaceuticals LLC | 72205-087 | 72205-0087-30 | — |
| Tiagabine Hydrochloride | Tiagabine hydrochloride 16 mg/1 | Tablet, Film coatedOral | Teva Pharmaceuticals USA, Inc. | 0093-8076 | 00093-8076-56 | — |
| Tiagabine Hydrochloride | Tiagabine hydrochloride 12 mg/1 | Tablet, Film coatedOral | Teva Pharmaceuticals USA, Inc. | 0093-8072 | 00093-8072-56 | — |
| Tiagabine Hydrochloride | Tiagabine hydrochloride 2 mg/1 | Tablet, Film coatedOral | Teva Pharmaceuticals USA, Inc. | 0093-5030 | 00093-5030-56 | — |
| Tiagabine Hydrochloride | Tiagabine hydrochloride 4 mg/1 | Tablet, Film coatedOral | Teva Pharmaceuticals USA, Inc. | 0093-5031 | 00093-5031-56 | — |
| Tiagabine Hydrochloride | Tiagabine hydrochloride 2 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 62756-200 | 62756-0200-1862756-0200-83 | — |
| Tiagabine Hydrochloride | Tiagabine hydrochloride 4 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 62756-224 | 62756-0224-0862756-0224-1862756-0224-83+1 more | — |
Tiagabine Hydrochloride: common questions
- What is the NDC for Tiagabine Hydrochloride?
- Tiagabine Hydrochloride has 10 product NDCs, one for each strength, dosage form and labeler; each product NDC then has one package NDC per package size. Pick the row for your product above to see its package NDCs.
- Is there a J-code for Tiagabine Hydrochloride?
- Med-Code's curated HCPCS directory has no drug-specific code for these products. Drugs dispensed by a pharmacy are billed by NDC. NDC vs J-code.
- Which NDC goes on a claim?
- The package NDC of what was given, in 11-digit form. How to convert a 10-digit NDC.